6ec6c29454ddc661b78710d1bb6de040cafaa66d
lrnassar
Sat Jun 13 09:39:33 2026 -0700
lrSv: remove premature per-track release tags that broke tdbQuery -strict. refs #36258
The hprc2JasmineSv and lrSv1kLin stanzas carried "release alpha", but the file
is pulled in via "include lrSv.ra alpha", and tdbQuery -check -strict rejects a
stanza-level release tag when the include line already supplies a release
override ("Release tag in stanza with include release override"). The
include-level alpha already keeps the entire supertrack on dev/alpha, so these
two unpublished subtracks do not graduate regardless. Per-track release tags
for the do-not-release subtracks should be added when the include line is later
changed past alpha.
diff --git src/hg/makeDb/trackDb/human/lrSv.ra src/hg/makeDb/trackDb/human/lrSv.ra
index 1a2afbf596e..e66a29dacc5 100644
--- src/hg/makeDb/trackDb/human/lrSv.ra
+++ src/hg/makeDb/trackDb/human/lrSv.ra
@@ -1,558 +1,556 @@
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|DEL (Deletion),INS|INS (Insertion),INV|INV (Inversion),CPX|CPX (Complex rearrangement),DUP|DUP (Duplication),CNV|CNV (Copy-number variant),CTX|CTX (Chromosomal translocation),INSDEL|INSDEL (Insertion-deletion),MIXED|MIXED (multi-allele snarl),BND|BND (Breakend / translocation),MEI|MEI (Mobile element insertion),TRA|TRA (Translocation)
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
include lrSvAll.ra
track colorsDbSv
parent lrSv
bigDataUrl /gbdb/$D/lrSv/colorsDb/sv.$D.bb
shortLabel CoLoRSdb 1427 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) svLen=$svLen insLen=$insLen AF=$AF AC=$AC/$AN (Hom:$acHom Het:$acHet Hemi:$acHemi) samples=$NS
searchIndex name
filterValues.svType DEL,INS,INV,DUP
filterType.svType multipleListOr
filterLabel.svType SV Type
filter.svLen 0:101381
filterByRange.svLen on
filterLabel.svLen SV Length (bp)
filter.insLen 0:18724
filterByRange.insLen on
filterLabel.insLen Insertion Length (bp)
filter.AC 0:2854
filterByRange.AC on
filterLabel.AC Alt Allele Count (AC)
filter.AF 0:1
filterByRange.AF on
filterLimits.AF 0:1
filterLabel.AF Allele Frequency (AF)
skipEmptyFields on
priority 1
track lrSv1kgOnt
parent lrSv
bigDataUrl /gbdb/$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>$name</b> ($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
filter.AC 0:1816
filterByRange.AC on
filterLabel.AC Allele Count
skipEmptyFields on
dataVersion 1.1
priority 2
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> ($svType) svLen=$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 1027 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) svLen=$svLen insLen=$insLen AC~$AC AF_AFR=$afAfr AF_EUR=$afEur
filterValues.svType DEL,INS
filterType.svType multipleListOr
filterLabel.svType SV Type
filter.svLen 0:9905
filterByRange.svLen on
filterLabel.svLen SV Length
filter.insLen 0:9998
filterByRange.insLen on
filterLabel.insLen Insertion Length
filter.AC 0:2054
filterByRange.AC on
filterLabel.AC Allele Count (approx)
filterByRange.afAfr on
filterLimits.afAfr 0:1
filterLabel.afAfr AF African
filterByRange.afEur on
filterLimits.afEur 0:1
filterLabel.afEur AF European
filterByRange.afEas on
filterLimits.afEas 0:1
filterLabel.afEas AF East Asian
skipEmptyFields on
track han945Sv
parent lrSv
bigDataUrl /gbdb/$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) 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 tommoJpSv
parent lrSv
bigDataUrl /gbdb/$D/lrSv/tommoJp.bb
shortLabel ToMMo 333 SVs
longLabel Structural Variants from 333 Japanese Individuals (ToMMo, 111 Trios)
type bigBed 9 +
itemRgb on
visibility dense
mouseOver <b>$name</b> ($svType) svLen=$svLen insLen=$insLen AF=$alleleFreq AC=$AC
filterValues.svType DEL,INS
filterType.svType multipleListOr
filterLabel.svType SV Type
filter.svLen 0:99985
filterByRange.svLen on
filterLabel.svLen SV Length
filter.insLen 0:30649
filterByRange.insLen on
filterLabel.insLen Insertion Length
filter.alleleFreq 0:1
filterByRange.alleleFreq on
filterLimits.alleleFreq 0:1
filterLabel.alleleFreq Allele Frequency
filter.AC 0:444
filterByRange.AC on
filterLabel.AC Allele Count
track ga4kSv
parent lrSv
bigDataUrl /gbdb/$D/lrSv/ga4kSv.bb
shortLabel GA4K 502 SVs
longLabel Structural Variants from 502 Children's Mercy GA4K Probands (PacBio HiFi)
type bigBed 9 +
itemRgb on
visibility dense
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/$D/lrSv/decodeSv.bb
shortLabel deCODE 3622 SVs
longLabel High-confidence Structural Variants from 3,622 Icelanders (deCODE, Oxford Nanopore)
type bigBed 9 +
itemRgb on
visibility dense
mouseOver <b>$name</b> ($svType) svLen=$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 hprc2v21Sv
parent lrSv
bigDataUrl /gbdb/$D/lrSv/hprc2v21.bb
shortLabel HPRC v2.1 233 SVs
longLabel Structural Variants from HPRC v2.1 Pangenome Graph (233 samples, minigraph-cactus)
type bigBed 9 +
itemRgb on
visibility dense
mouseOver <b>$name</b> ($svType) svLen=$svLen insLen=$insLen AF=$alleleFreq AC=$AC/$alleleNumber samples=$nSamples
filterValues.svType INS,DEL
filterType.svType multipleListOr
filterLabel.svType SV Type
filter.svLen 0:99835
filterByRange.svLen on
filterLabel.svLen SV Length
filter.insLen 0:1064897
filterByRange.insLen on
filterLabel.insLen Insertion Length
filter.AC 0:463
filterByRange.AC on
filterLabel.AC Allele Count
filter.alleleFreq 0:1
filterByRange.alleleFreq on
filterLimits.alleleFreq 0:1
filterLabel.alleleFreq Allele Frequency
filter.snarlLevel 0:7
filterByRange.snarlLevel on
filterLabel.snarlLevel Snarl Level
skipEmptyFields on
track hprc2JasmineSv
parent lrSv
- release alpha
bigDataUrl /gbdb/$D/lrSv/hprc2Jasmine.bb
shortLabel HPRC2 Jasmine 231 SVs
longLabel Structural Variants from 231 HPRC v2 Assemblies (Jasmine merge of 14 SV callers)
type bigBed 9 +
itemRgb on
visibility dense
mouseOver <b>$name</b> ($svType) svLen=$svLen insLen=$insLen samples=$nSamples/$alleleNumber AF=$alleleFreq callers=$nCallers ($callers)
filterValues.svType DEL,INS
filterType.svType multipleListOr
filterLabel.svType SV Type
filter.svLen 0:30176500
filterByRange.svLen on
filterLabel.svLen SV Length
filter.insLen 0:30176500
filterByRange.insLen on
filterLabel.insLen Insertion Length
filter.AC 0:231
filterByRange.AC on
filterLabel.AC Carrier Sample Count
filter.alleleFreq 0:1
filterByRange.alleleFreq on
filterLimits.alleleFreq 0:1
filterLabel.alleleFreq Carrier Frequency
filter.nCallers 1:14
filterByRange.nCallers on
filterLabel.nCallers Number of Supporting Callers
filterValues.callers DELLY,DeBreak,DeepVariant,PAV,SVDSS,SVIM,SVIM-asm,Sniffles2,cuteSV,cuteSV-asm,dipcall,longcallD,pbsv,sawfish
filterType.callers multipleListAnd
filterLabel.callers Supporting Callers
filterValues.sources PAV,dipcall,longcallD
filterType.sources multipleListAnd
filterLabel.sources Source Pipeline
skipEmptyFields on
track hgsvc2Sv
parent lrSv
bigDataUrl /gbdb/$D/lrSv/hgsvc2.bb
shortLabel HGSVC2 32 SVs
longLabel Structural Variants from 32 Haplotype-Resolved Genomes (HGSVC2 freeze 4, Ebert 2021)
type bigBed 9 +
itemRgb on
visibility dense
mouseOver <b>$name</b> ($svType) svLen=$svLen insLen=$insLen samples=$sampleCount AC=$AC AF=$popAllAf
filterValues.svType DEL,INS,INV
filterType.svType multipleListOr
filterLabel.svType SV Type
filter.svLen 0:57207414
filterByRange.svLen on
filterLabel.svLen SV Length
filter.insLen 0:108546
filterByRange.insLen on
filterLabel.insLen Insertion Length
filter.AC 1:35
filterByRange.AC on
filterLabel.AC Allele Count (carrier haplotypes)
filter.sampleCount 1:35
filterByRange.sampleCount on
filterLabel.sampleCount Sample Count
filterValues.refTrf True,False
filterType.refTrf multipleListOr
filterLabel.refTrf In Tandem Repeat
filter.refSd 0:1
filterByRange.refSd on
filterLimits.refSd 0:1
filterLabel.refSd Segmental Duplication Overlap
skipEmptyFields on
track hgsvc3Sv
parent lrSv
bigDataUrl /gbdb/$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) 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.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/$D/lrSv/kwanho.bb
shortLabel Kim PD 100 prelim
longLabel Structural Variants from 100 Post-mortem Brains (Parkinson's disease, ILBD, Control; Kim et al. 2026, PacBio HiFi) - PRELIMINARY, data to be updated, contact the authors before using
type bigBed 9 +
itemRgb on
visibility dense
mouseOver <b>$name</b> ($svType) svLen=$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 the Arab Pangenome Reference (53 UAE-resident Arab samples)
type bigBed 9 +
itemRgb on
visibility dense
mouseOver <b>$name</b> ($svType) svLen=$svLen insLen=$insLen AC=$AC/$alleleNumber AF=$alleleFreq samples=$numSamples alts=$numAlts
filterValues.svType INS,DEL,CPX,MIXED
filterType.svType multipleListOr
filterLabel.svType SV Type
filter.svLen 0:99885
filterByRange.svLen on
filterLabel.svLen SV Length
filter.insLen 0:584016
filterByRange.insLen on
filterLabel.insLen Insertion Length
filter.AC 0:107
filterByRange.AC on
filterLabel.AC Allele Count
filterByRange.alleleFreq on
filterLimits.alleleFreq 0:1
filterLabel.alleleFreq Allele Frequency
skipEmptyFields on
track cpc1Sv
parent lrSv
bigDataUrl /gbdb/$D/lrSv/cpc1.bb
shortLabel CPC 58 SVs
longLabel Structural Variants from the Chinese Pangenome Consortium (58 samples, CPC-only)
type bigBed 9 +
itemRgb on
visibility dense
mouseOver <b>$name</b> ($svType) svLen=$svLen insLen=$insLen AC=$AC/$alleleNumber AF=$alleleFreq samples=$numSamples alts=$numAlts
filterValues.svType INS,DEL,CPX,MIXED
filterType.svType multipleListOr
filterLabel.svType SV Type
filter.svLen 0:8998096
filterByRange.svLen on
filterLabel.svLen SV Length
filter.insLen 0:376583
filterByRange.insLen on
filterLabel.insLen Insertion Length
filter.AC 0:116
filterByRange.AC on
filterLabel.AC Allele Count
filterByRange.alleleFreq on
filterLimits.alleleFreq 0:1
filterLabel.alleleFreq Allele Frequency
skipEmptyFields on
track chirmade101Sv
parent lrSv
bigDataUrl /gbdb/$D/lrSv/chirmade101.bb
shortLabel SVatalog 101 SVs
longLabel Structural Variants from 101 Long-read WGS (GWAS SVatalog, Chirmade 2026)
type bigBed 9 +
itemRgb on
visibility dense
mouseOver <b>$name</b> ($svType) svLen=$svLen insLen=$insLen genes=$geneCount
filterValues.svType DEL,INS,DUP,INV,CPX
filterType.svType multipleListOr
filterLabel.svType SV Type
filter.svLen 0:1321484
filterByRange.svLen on
filterLabel.svLen SV Length
filter.insLen 0:31711
filterByRange.insLen on
filterLabel.insLen Insertion Length
filter.geneCount 0:200
filterByRange.geneCount on
filterLabel.geneCount Gene Count
skipEmptyFields on
# NOT FOR RELEASE: data received from Eichler lab via email, not yet published.
# Do not add to lrSvAll merged track until a preprint or paper is available.
track lrSv1kLin
parent lrSv
- release alpha
bigDataUrl /gbdb/$D/lrSv/lin1218.bb
shortLabel 1KG Linear 1218 SVs
longLabel Structural Variants from 1,218 Individuals (1000 Genomes, Linear Long-read)
type bigBed 9 +
itemRgb on
visibility dense
mouseOver <b>$name</b> ($svType) svLen=$svLen insLen=$insLen AC=$AC/$AN AF=$AF AF_AFR=$afAfr AF_EUR=$afEur samples=$NS
searchIndex name
filterValues.svType DEL,INS
filterType.svType multipleListOr
filterLabel.svType SV Type
filter.svLen 0:99565
filterByRange.svLen on
filterLabel.svLen SV Length (bp)
filter.insLen 0:99968
filterByRange.insLen on
filterLabel.insLen Insertion Length (bp)
filter.AC 0:2436
filterByRange.AC on
filterLabel.AC Allele Count
filter.AF 0:1
filterByRange.AF on
filterLimits.AF 0:1
filterLabel.AF Allele Frequency
filterByRange.afAfr on
filterLimits.afAfr 0:1
filterLabel.afAfr AF African
filterByRange.afAmr on
filterLimits.afAmr 0:1
filterLabel.afAmr AF Admixed American
filterByRange.afEas on
filterLimits.afEas 0:1
filterLabel.afEas AF East Asian
filterByRange.afEur on
filterLimits.afEur 0:1
filterLabel.afEur AF European
filterByRange.afSas on
filterLimits.afSas 0:1
filterLabel.afSas AF South Asian
filter.NS 1:1218
filterByRange.NS on
filterLabel.NS Samples with Genotype Data
skipEmptyFields on