1732661494ece5e645a9522f15a0f5922b035d1a max Wed Apr 22 08:57:11 2026 -0700 colorsDbSv: rebuild from pbsv+Jasmine source VCFs with richer AS Rebuild the CoLoRSdb SV bigBeds for hg38 and hs1 from the upstream pbsv+Jasmine VCFs that the CoLoRSdb project distributes directly. The previous bigBed stored AF as a string (breaking the numeric filter) and lacked insLen (causing a "filter on field insLen not in AS file" error under the supertrack-level filter). The new build: - stores AF as a float - adds a derived insLen column (alt-ref length delta for INS, 0 otherwise) so the shared lrSv insLen filter applies - keeps every INFO field from the source (SVTYPE, SVLEN, END, AC, AN, NS, AC_Hom, AC_Het, AC_Hemi, AF, HWE, ExcHet, nhomalt) plus REF/ALT - uses the canonical svName(TYPE, featLen, AC) label via lrSvCommon Record counts match the source VCFs: 426,239 on hg38 (59 MB) and 839,714 on hs1 (87 MB). /gbdb symlinks unchanged. The trackDb colorsDbSv stanza is updated to reference the new AS field names (acHom/acHet/acHemi, AF, AN) and to add the insLen filter. Also fixes a nearby `version 1.1` -> `dataVersion 1.1` typo in lrSv1kgOnt that was failing the tagTypes check. refs #36258 diff --git src/hg/makeDb/trackDb/human/lrSv.ra src/hg/makeDb/trackDb/human/lrSv.ra index ca027b343a1..a1fd5e56ed5 100644 --- src/hg/makeDb/trackDb/human/lrSv.ra +++ src/hg/makeDb/trackDb/human/lrSv.ra @@ -1,483 +1,584 @@ track lrSv superTrack on shortLabel Long-read SVs longLabel Structural Variants from Long-read Sequencing group varRep visibility hide +# Supertrack-level filters. These are rendered on the supertrack's own +# hgTrackUi page (superTrackUi in hgTrackUi.c). Cart values stored under +# "lrSv.filter.<field>.min/max" are inherited at read time by every +# subtrack via cartOptionalStringClosestToHome() walking tdb->parent. A +# subtrack-level filter always wins over the supertrack-level one. +filterValues.svType DEL,INS,INV,CPX,DUP,CNV,CTX,INSDEL,MIXED,BND,MEI,TRA +filterType.svType multipleListOr +filterLabel.svType SV Type +filter.svLen 0:250000000 +filterByRange.svLen on +filterLabel.svLen SV Length (bp) +filter.insLen 0:30176500 +filterByRange.insLen on +filterLabel.insLen Insertion Length (bp) +filter.AC 0:30000 +filterByRange.AC on +filterLabel.AC Allele Count +noScoreFilter on track colorsDbSv parent lrSv bigDataUrl /gbdb/$D/lrSv/colorsDb/sv.$D.bb shortLabel CoLoRSdb 1,427 SVs longLabel Structural Variants from CoLoRSdb (Consortium of Long-Read Sequencing, 1,427 Samples) type bigBed 9 + itemRgb on visibility dense dataVersion v1.2.0 - mouseOver <b>$name</b> ($svType) len=$svLen AF=$af AC=$AC (Hom:$AC_Hom Het:$AC_Het Hemi:$AC_Hemi) samples=$NS + mouseOver <b>$name</b> ($svType) svLen=$svLen insLen=$insLen AF=$AF AC=$AC/$AN (Hom:$acHom Het:$acHet Hemi:$acHemi) samples=$NS searchIndex name - filterValues.svType DEL,INS,INV + filterValues.svType DEL,INS,INV,DUP filterType.svType multipleListOr filterLabel.svType SV Type - filter.svLen 20:101381 + filter.svLen 0:101381 filterByRange.svLen on - filterLabel.svLen SV Length + filterLabel.svLen SV Length (bp) + filter.insLen 0:18724 + filterByRange.insLen on + filterLabel.insLen Insertion Length (bp) filter.AC 0:2854 filterByRange.AC on filterLabel.AC Alt Allele Count (AC) + filter.AF 0:1 + filterByRange.AF on + filterLimits.AF 0:1 + filterLabel.AF Allele Frequency (AF) skipEmptyFields on priority 1 track lrSv1kgOnt parent lrSv bigDataUrl /gbdb/$D/lrSv/1kgOnt.bb shortLabel 1KG ONT 1019 SVs longLabel Structural Variants from 1,019 Diverse Humans (Vienna ONT, Schloissnig et al. 2025) type bigBed 9 + itemRgb on visibility dense - mouseOver <b>$name</b> ($svClass) len=$svLen type=$insType family=$family AC=$alleleCount AF=$alleleFreq - filterValues.svClass DEL,INS,COMPLEX - filterType.svClass multipleListOr - filterLabel.svClass SV Class + mouseOver <b>$name</b> ($svType) svLen=$svLen insLen=$insLen type=$insType family=$family AC=$AC AF=$alleleFreq + filterValues.svType DEL,INS,CPX + filterType.svType multipleListOr + filterLabel.svType SV Type filterValues.insType COMPLEX_DUP,DUP,DUP_INTERSPERSED,INV_DUP,NUMT,PSD,VNTR,chimera,orphan,partnered,solo filterType.insType multipleListOr filterLabel.insType Insertion/Deletion Type filterValues.family Alu,HERVK,L1,LTR5_Hs,SVA filterType.family multipleListOr filterLabel.family Transposon Family + filter.svLen 0:49171 filterByRange.svLen on filterLabel.svLen SV Length + filter.insLen 0:48091 + filterByRange.insLen on + filterLabel.insLen Insertion Length filterByRange.alleleFreq on filterLimits.alleleFreq 0:1 filterLabel.alleleFreq Allele Frequency - filterByRange.alleleCount on - filterLabel.alleleCount Allele Count + filter.AC 0:1816 + filterByRange.AC on + filterLabel.AC Allele Count skipEmptyFields on + dataVersion 1.1 priority 2 track abelSv parent lrSv bigDataUrl /gbdb/$D/abelSv/abelSv.bb shortLabel CCDG 17795 SR SVs longLabel Structural Variants from 17,795 Genomes - Illumina SHORT-READ CCDG callset (Abel et al. 2020) - included for comparison type bigBed 9 + itemRgb on visibility dense - mouseOver <b>$name</b> ($svType) len=$svLength AF=$af AC=$ac/$an callset=$callset MSQ=$msq + mouseOver <b>$name</b> ($svType) svLen=$svLen insLen=$insLen AF=$af AC=$AC/$an callset=$callset MSQ=$msq skipEmptyFields on skipFields mateChrom,matePos filterValues.svType DEL|deletion,DUP|duplication,INV|inversion,MEI|mobile element insertion,BND|breakend/translocation filterType.svType multipleListOr filterLabel.svType SV Type filterValues.callset B38|Native GRCh38 callset (14623 samples),B37lift|Lifted from GRCh37 callset (8417 samples) filterType.callset multipleListOr filterLabel.callset Source Callset filterValues.filter PASS|High confidence,LOW|Low confidence filterType.filter multipleListOr filterLabel.filter Filter Status filterByRange.af on filter.af 0:1 filterLimits.af 0:1 filterLabel.af Allele Frequency (AF) - filterByRange.svLength on - filter.svLength 0:250000000 - filterLimits.svLength -1:250000000 - filterLabel.svLength SV Length (bp; -1 for BND) + filterByRange.svLen on + filter.svLen 0:250000000 + filterLimits.svLen -1:250000000 + filterLabel.svLen SV Length (bp; -1 for BND) + filter.insLen 0:8545 + filterByRange.insLen on + filterLabel.insLen Insertion Length filterByRange.msq on filter.msq 0:500 filterLimits.msq 0:500 filterLabel.msq Mean Sample Quality (MSQ) - filterByRange.ac on - filter.ac 0:30000 - filterLimits.ac 0:30000 - filterLabel.ac Allele Count (AC) + filterByRange.AC on + filter.AC 0:30000 + filterLimits.AC 0:30000 + filterLabel.AC Allele Count (AC) url https://www.nature.com/articles/s41586-020-2371-0 urlLabel Abel et al, Nature 2020: track onekg3202Sr parent lrSv bigDataUrl /gbdb/$D/lrSv/onekg3202sr.bb shortLabel 1KG 3202 SR SVs longLabel 1000 Genomes 3202-sample Illumina SHORT-READ GATK-SV callset (Byrska-Bishop 2022) - included for comparison type bigBed 9 + itemRgb on visibility dense - mouseOver <b>$name</b> ($svType) len=$svLen AF=$alleleFreq AC=$alleleCount/$alleleNumber popMax=$popmaxAf + mouseOver <b>$name</b> ($svType) svLen=$svLen insLen=$insLen AF=$alleleFreq AC=$AC/$alleleNumber popMax=$popmaxAf filterValues.svType DEL,INS,DUP,INV,CPX,CTX,CNV filterType.svType multipleListOr filterLabel.svType SV Type filter.svLen 0:154807729 filterByRange.svLen on filterLabel.svLen SV Length + filter.insLen 0:178243 + filterByRange.insLen on + filterLabel.insLen Insertion Length + filter.AC 0:6404 + filterByRange.AC on + filterLabel.AC Allele Count filter.alleleFreq 0:1 filterByRange.alleleFreq on filterLimits.alleleFreq 0:1 filterLabel.alleleFreq Allele Frequency (all) filter.popmaxAf 0:1 filterByRange.popmaxAf on filterLimits.popmaxAf 0:1 filterLabel.popmaxAf Population Max AF filter.afAfr 0:1 filterByRange.afAfr on filterLimits.afAfr 0:1 filterLabel.afAfr AF African filter.afEur 0:1 filterByRange.afEur on filterLimits.afEur 0:1 filterLabel.afEur AF European skipEmptyFields on track gustafsonSv parent lrSv bigDataUrl /gbdb/$D/lrSv/gustafson.bb shortLabel 1KG ONT 100 SVs longLabel Structural Variants from 100 1000 Genomes ONT Samples (Gustafson et al. 2024) type bigBed 9 + itemRgb on visibility dense - mouseOver <b>$name</b> ($svType) len=$svLen samples=$sampleCount + mouseOver <b>$name</b> ($svType) svLen=$svLen insLen=$insLen AC=$AC samples=$sampleCount filterValues.svType DEL,INS,DUP,INV filterType.svType multipleListOr filterLabel.svType SV Type filter.svLen 0:98289 filterByRange.svLen on filterLabel.svLen SV Length + filter.insLen 0:25094 + filterByRange.insLen on + filterLabel.insLen Insertion Length + filter.AC 0:200 + filterByRange.AC on + filterLabel.AC Allele Count (placeholder) filter.sampleCount 1:100 filterByRange.sampleCount on filterLabel.sampleCount Number of Carrier Samples skipEmptyFields on priority 3 track aou1kSv parent lrSv bigDataUrl /gbdb/$D/lrSv/aou1k.bb shortLabel AoU 1K SVs longLabel Structural Variants from 1,027 AoU Individuals (PacBio HiFi Long-read) type bigBed 9 + itemRgb on visibility dense - mouseOver <b>$name</b> ($svType) len=$svLen AF_AFR=$afAfr AF_EUR=$afEur + mouseOver <b>$name</b> ($svType) svLen=$svLen insLen=$insLen AC~$AC AF_AFR=$afAfr AF_EUR=$afEur filterValues.svType DEL,INS filterType.svType multipleListOr filterLabel.svType SV Type - #filter.svLen 50:9998 + filter.svLen 0:9905 filterByRange.svLen on filterLabel.svLen SV Length - #filter.afAfr 0:1 + filter.insLen 0:9998 + filterByRange.insLen on + filterLabel.insLen Insertion Length + filter.AC 0:2054 + filterByRange.AC on + filterLabel.AC Allele Count (approx) filterByRange.afAfr on filterLimits.afAfr 0:1 filterLabel.afAfr AF African - #filter.afEur 0:1 filterByRange.afEur on filterLimits.afEur 0:1 filterLabel.afEur AF European - #filter.afEas 0:1 filterByRange.afEas on filterLimits.afEas 0:1 filterLabel.afEas AF East Asian skipEmptyFields on track han945Sv parent lrSv bigDataUrl /gbdb/$D/lrSv/han945.bb shortLabel Han 945 SVs longLabel Structural Variants from 945 Han Chinese (Long-read Sequencing) type bigBed 9 + itemRgb on visibility dense - mouseOver <b>$name</b> ($svType) len=$svLen AF=$alleleFreq samples=$sampleCount + mouseOver <b>$name</b> ($svType) svLen=$svLen insLen=$insLen AF=$alleleFreq AC=$AC samples=$sampleCount filterValues.svType DEL,INS,DUP,INV,TRA filterType.svType multipleListOr filterLabel.svType SV Type filter.svLen 0:99743 filterByRange.svLen on filterLabel.svLen SV Length + filter.insLen 0:27242 + filterByRange.insLen on + filterLabel.insLen Insertion Length + filter.AC 0:1890 + filterByRange.AC on + filterLabel.AC Allele Count (approx 2*SUPP) filter.sampleCount 1:945 filterByRange.sampleCount on filterLabel.sampleCount Number of Supporting Samples filter.alleleFreq 0:1 filterByRange.alleleFreq on filterLimits.alleleFreq 0:1 filterLabel.alleleFreq Allele Frequency skipEmptyFields on urls chr2="hgTracks?position=$$" track tommoJpCnv parent lrSv container multiWig aggregate transparentOverlay showSubtrackColorOnUi on shortLabel ToMMo 48K CNV SR longLabel CNV Carrier Counts from 48,874 Japanese Individuals (ToMMo 48KJPN-CNV, short-read WGS; 1 kb bins) - included for comparison type bigWig 0 48874 autoScale on viewLimits 0:1000 viewLimitsMax 0:48874 maxHeightPixels 100:32:8 visibility full priority 2.5 track tommoJpCnvLoss parent tommoJpCnv bigDataUrl /gbdb/$D/lrSv/tommoJpCnvLoss.bw shortLabel ToMMo CNV Loss longLabel Samples with copy-number loss (CN<2) per 1 kb bin, ToMMo 48KJPN-CNV type bigWig 0 48874 color 200,0,0 altColor 200,0,0 track tommoJpCnvGain parent tommoJpCnv bigDataUrl /gbdb/$D/lrSv/tommoJpCnvGain.bw shortLabel ToMMo CNV Gain longLabel Samples with copy-number gain (CN>2) per 1 kb bin, ToMMo 48KJPN-CNV type bigWig 0 48874 color 0,160,0 altColor 0,160,0 track tommoJpSv parent lrSv bigDataUrl /gbdb/$D/lrSv/tommoJp.bb shortLabel ToMMo Japanese SVs longLabel Structural Variants from 333 Japanese Individuals (ToMMo, 111 Trios) type bigBed 9 + itemRgb on visibility dense - mouseOver <b>$name</b> ($svType) len=$svLen AF=$alleleFreq AC=$alleleCount + mouseOver <b>$name</b> ($svType) svLen=$svLen insLen=$insLen AF=$alleleFreq AC=$AC filterValues.svType DEL,INS filterType.svType multipleListOr filterLabel.svType SV Type - filter.svLen 51:99980 + filter.svLen 0:99985 filterByRange.svLen on filterLabel.svLen SV Length + filter.insLen 0:30649 + filterByRange.insLen on + filterLabel.insLen Insertion Length filter.alleleFreq 0:1 filterByRange.alleleFreq on filterLimits.alleleFreq 0:1 filterLabel.alleleFreq Allele Frequency - filter.alleleCount 0:444 - filterByRange.alleleCount on - filterLabel.alleleCount Allele Count + filter.AC 0:444 + filterByRange.AC on + filterLabel.AC Allele Count track ga4kSv parent lrSv bigDataUrl /gbdb/$D/lrSv/ga4kSv.bb shortLabel GA4K SVs longLabel Structural Variants from 502 Children's Mercy GA4K Probands and Families (PacBio HiFi) type bigBed 9 + itemRgb on visibility dense - mouseOver <b>$name</b> ($svType) len=$svLen AF=$alleleFreq carriers=$carrierCount/$sampleTotal + mouseOver <b>$name</b> ($svType) svLen=$svLen insLen=$insLen AC~$AC AF=$alleleFreq carriers=$carrierCount/$sampleTotal filterValues.svType DEL,INS,DUP,INV filterType.svType multipleListOr filterLabel.svType SV Type filter.svLen 0:809711 filterByRange.svLen on filterLabel.svLen SV Length + filter.insLen 0:14923 + filterByRange.insLen on + filterLabel.insLen Insertion Length + filter.AC 0:996 + filterByRange.AC on + filterLabel.AC Allele Count (approx) filter.alleleFreq 0:1 filterByRange.alleleFreq on filterLimits.alleleFreq 0:1 filterLabel.alleleFreq Allele Frequency filter.carrierCount 1:498 filterByRange.carrierCount on filterLabel.carrierCount Number of Carrier Samples track decodeSv parent lrSv bigDataUrl /gbdb/$D/lrSv/decodeSv.bb shortLabel deCODE 3,622 SVs longLabel High-confidence Structural Variants from 3,622 Icelanders (deCODE, Oxford Nanopore) type bigBed 9 + itemRgb on visibility dense - mouseOver <b>$name</b> ($svType) len=$svLen + mouseOver <b>$name</b> ($svType) svLen=$svLen insLen=$insLen AC=$AC (placeholder) filterValues.svType DEL,INS,INSDEL filterType.svType multipleListOr filterLabel.svType SV Type filter.svLen 0:861080 filterByRange.svLen on filterLabel.svLen SV Length + filter.insLen 0:22130 + filterByRange.insLen on + filterLabel.insLen Insertion Length + filter.AC 0:50 + filterByRange.AC on + filterLabel.AC Allele Count (placeholder 50) skipEmptyFields on track hprc2Sv parent lrSv bigDataUrl /gbdb/$D/lrSv/hprc2.bb shortLabel HPRC v2 SVs longLabel Structural Variants from the HPRC v2 Pangenome Graph (233 Samples, minigraph-cactus + vcfwave) type bigBed 9 + itemRgb on visibility dense - mouseOver <b>$name</b> ($svType) len=$svLen AF=$alleleFreq AC=$alleleCount/$alleleNumber samples=$nSamples - filterValues.svType INS,DEL,COMPLEX,INV + mouseOver <b>$name</b> ($svType) svLen=$svLen insLen=$insLen AF=$alleleFreq AC=$AC/$alleleNumber samples=$nSamples + filterValues.svType INS,DEL,CPX,INV filterType.svType multipleListOr filterLabel.svType SV Type - filter.svLen 50:97718 + filter.svLen 0:99113 filterByRange.svLen on filterLabel.svLen SV Length + filter.insLen 0:97718 + filterByRange.insLen on + filterLabel.insLen Insertion Length + filter.AC 0:463 + filterByRange.AC on + filterLabel.AC Allele Count filter.alleleFreq 0:1 filterByRange.alleleFreq on filterLimits.alleleFreq 0:1 filterLabel.alleleFreq Allele Frequency filter.snarlLevel 0:10 filterByRange.snarlLevel on filterLabel.snarlLevel Snarl Level skipEmptyFields on track hgsvc2Sv parent lrSv bigDataUrl /gbdb/$D/lrSv/hgsvc2.bb shortLabel HGSVC2 32 SVs longLabel Structural Variants from 32 Haplotype-Resolved Genomes (HGSVC2 freeze 4, Ebert et al. 2021) type bigBed 9 + itemRgb on visibility dense - mouseOver <b>$name</b> ($svType) len=$svLen samples=$sampleCount alleles=$alleleCount AF=$popAllAf + mouseOver <b>$name</b> ($svType) svLen=$svLen insLen=$insLen samples=$sampleCount AC=$AC AF=$popAllAf filterValues.svType DEL,INS,INV filterType.svType multipleListOr filterLabel.svType SV Type filter.svLen 0:57207414 filterByRange.svLen on filterLabel.svLen SV Length - filter.alleleCount 1:35 - filterByRange.alleleCount on - filterLabel.alleleCount Allele Count (carrier haplotypes) + filter.insLen 0:108546 + filterByRange.insLen on + filterLabel.insLen Insertion Length + filter.AC 1:35 + filterByRange.AC on + filterLabel.AC Allele Count (carrier haplotypes) filter.sampleCount 1:35 filterByRange.sampleCount on filterLabel.sampleCount Sample Count filterValues.refTrf True,False filterType.refTrf multipleListOr filterLabel.refTrf In Tandem Repeat filter.refSd 0:1 filterByRange.refSd on filterLimits.refSd 0:1 filterLabel.refSd Segmental Duplication Overlap skipEmptyFields on track hgsvc3Sv parent lrSv bigDataUrl /gbdb/$D/lrSv/hgsvc3.bb shortLabel HGSVC3 65 SVs longLabel Structural Variants from 65 Diverse Samples (HGSVC3 ONT+HIFI) type bigBed 9 + itemRgb on visibility dense - mouseOver <b>$name</b> ($svType) len=$svLen samples=$sampleCount alleles=$alleleCount + mouseOver <b>$name</b> ($svType) svLen=$svLen insLen=$insLen samples=$sampleCount AC=$AC filterValues.svType DEL,INS,INV filterType.svType multipleListOr filterLabel.svType SV Type filter.svLen 0:30176500 filterByRange.svLen on filterLabel.svLen SV Length - filter.alleleCount 1:136 - filterByRange.alleleCount on - filterLabel.alleleCount Allele Count (carrier haplotypes) + filter.insLen 0:30176500 + filterByRange.insLen on + filterLabel.insLen Insertion Length + filter.AC 1:136 + filterByRange.AC on + filterLabel.AC Allele Count (carrier haplotypes) filter.sampleCount 1:65 filterByRange.sampleCount on filterLabel.sampleCount Sample Count filterValues.refTrf True,False filterType.refTrf multipleListOr filterLabel.refTrf In Tandem Repeat filter.refSd 0:1 filterByRange.refSd on filterLimits.refSd 0:1 filterLabel.refSd Segmental Duplication Overlap skipEmptyFields on track kwanhoSv parent lrSv bigDataUrl /gbdb/$D/lrSv/kwanho.bb shortLabel Kim PD Brain SVs (preliminary) longLabel Structural Variants from 100 Post-mortem Brains (Parkinson's disease, ILBD, Control; Kim et al. 2026, PacBio HiFi) - PRELIMINARY, data to be updated, contact the authors before using type bigBed 9 + itemRgb on visibility dense - mouseOver <b>$name</b> ($svType) len=$svLen AF_PD=$afPd AF_HC=$afHc diff=$differentialRate + mouseOver <b>$name</b> ($svType) svLen=$svLen insLen=$insLen AC=$AC AF_PD=$afPd AF_HC=$afHc diff=$differentialRate filterValues.svType DEL,INS,DUP,INV filterType.svType multipleListOr filterLabel.svType SV Type filter.svLen 0:200000000 filterByRange.svLen on filterLabel.svLen SV Length + filter.insLen 0:20145 + filterByRange.insLen on + filterLabel.insLen Insertion Length + filter.AC 0:200 + filterByRange.AC on + filterLabel.AC Allele Count (PD+HC+ILBD) filter.qual 0:100 filterByRange.qual on filterLabel.qual Quality filter.afPd 0:1 filterByRange.afPd on filterLimits.afPd 0:1 filterLabel.afPd Allele Frequency (PD) filter.afHc 0:1 filterByRange.afHc on filterLimits.afHc 0:1 filterLabel.afHc Allele Frequency (HC) filter.afIlbd 0:1 filterByRange.afIlbd on filterLimits.afIlbd 0:1 filterLabel.afIlbd Allele Frequency (ILBD) filter.differentialRate -1:1 filterByRange.differentialRate on filterLimits.differentialRate -1:1 filterLabel.differentialRate Case-Control Differential (case - control) skipEmptyFields on track aprSv parent lrSv bigDataUrl /gbdb/$D/lrSv/apr.bb shortLabel Arab APR 53 SVs longLabel Structural Variants from Arabic Pangenome Reference (53 UAE-resident Arab samples) type bigBed 9 + itemRgb on visibility dense - mouseOver <b>$name</b> ($svType) len=$svLen AC=$alleleCount/$alleleNumber AF=$alleleFreq samples=$numSamples alts=$numAlts + mouseOver <b>$name</b> ($svType) svLen=$svLen insLen=$insLen AC=$AC/$alleleNumber AF=$alleleFreq samples=$numSamples alts=$numAlts filterValues.svType INS,DEL,CPX,MIXED filterType.svType multipleListOr filterLabel.svType SV Type + filter.svLen 0:99885 filterByRange.svLen on filterLabel.svLen SV Length + filter.insLen 0:584016 + filterByRange.insLen on + filterLabel.insLen Insertion Length + filter.AC 0:107 + filterByRange.AC on + filterLabel.AC Allele Count filterByRange.alleleFreq on filterLimits.alleleFreq 0:1 filterLabel.alleleFreq Allele Frequency - filterByRange.alleleCount on - filterLabel.alleleCount Allele Count skipEmptyFields on track cpc1Sv parent lrSv bigDataUrl /gbdb/$D/lrSv/cpc1.bb shortLabel CPC 58 SVs longLabel Structural Variants from Chinese Pangenome Consortium (58 samples, CPC portion of the CPC+HPRC graph; HPRC-specific SVs removed) type bigBed 9 + itemRgb on visibility dense - mouseOver <b>$name</b> ($svType) len=$svLen AC=$alleleCount/$alleleNumber AF=$alleleFreq samples=$numSamples alts=$numAlts + mouseOver <b>$name</b> ($svType) svLen=$svLen insLen=$insLen AC=$AC/$alleleNumber AF=$alleleFreq samples=$numSamples alts=$numAlts filterValues.svType INS,DEL,CPX,MIXED filterType.svType multipleListOr filterLabel.svType SV Type + filter.svLen 0:8998096 filterByRange.svLen on filterLabel.svLen SV Length + filter.insLen 0:376583 + filterByRange.insLen on + filterLabel.insLen Insertion Length + filter.AC 0:116 + filterByRange.AC on + filterLabel.AC Allele Count filterByRange.alleleFreq on filterLimits.alleleFreq 0:1 filterLabel.alleleFreq Allele Frequency - filterByRange.alleleCount on - filterLabel.alleleCount Allele Count skipEmptyFields on track chirmade101Sv parent lrSv bigDataUrl /gbdb/$D/lrSv/chirmade101.bb shortLabel SVatalog 101 SVs longLabel Structural Variants from 101 Long-read Whole-Genome Sequences (GWAS SVatalog, Chirmade et al. 2026) type bigBed 9 + itemRgb on visibility dense - mouseOver <b>$name</b> ($svType) len=$svLen genes=$geneCount - filterValues.svType del,ins,dup,inv,complex + mouseOver <b>$name</b> ($svType) svLen=$svLen insLen=$insLen genes=$geneCount + filterValues.svType DEL,INS,DUP,INV,CPX filterType.svType multipleListOr filterLabel.svType SV Type filter.svLen 0:1321484 filterByRange.svLen on filterLabel.svLen SV Length + filter.insLen 0:31711 + filterByRange.insLen on + filterLabel.insLen Insertion Length filter.geneCount 0:200 filterByRange.geneCount on filterLabel.geneCount Gene Count skipEmptyFields on