44c00f07b0e94306e09f30c84ea6ab0f044e1a29
max
  Fri Aug 14 05:09:12 2026 -0700
adding lin et al long-read SV subtrack, refs #38099

diff --git src/hg/makeDb/trackDb/human/lrSv.ra src/hg/makeDb/trackDb/human/lrSv.ra
index b19c31b037b..11a432fa725 100644
--- src/hg/makeDb/trackDb/human/lrSv.ra
+++ src/hg/makeDb/trackDb/human/lrSv.ra
@@ -17,123 +17,124 @@
 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 longReadVariants
+    priority 1
     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)
+    longLabel Structural Variants from 1,427 CoLoRSdb samples (Consortium of Long-Read Sequencing, PacBio HiFi)
     type bigBed 9 +
     itemRgb on
     visibility hide
     dataVersion v1.2.0
     mouseOver <b>Var</b>: $name ($svType)<br><b>SV len</b>: $svLen<br><b>Ins len</b>: $insLen<br><b>AF</b>: $AF<br><b>AC</b>: $AC/$AN (Hom $acHom, Het $acHet, Hemi $acHemi)<br><b>Samples</b>: $NS
     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 longReadVariants
+    priority 4
     bigDataUrl /gbdb/$D/lrSv/1kgOnt.bb
-    shortLabel 1KG ONT 1019 SVs
-    longLabel Structural Variants from 1000 Genomes Vienna ONT - 1,019 genomes (Schloissnig et al. 2025)
+    shortLabel 1KG Vienna ONT SVs
+    longLabel Structural Variants from 1,019 1000 Genomes samples (Vienna ONT; Schloissnig et al. 2025)
     type bigBed 9 +
     itemRgb on
     visibility hide
     mouseOver <b>Var</b>: $name ($svType)<br><b>SV len</b>: $svLen<br><b>Ins len</b>: $insLen<br><b>Type</b>: $insType<br><b>Family</b>: $family<br><b>AC</b>: $AC<br><b>AF</b>: $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 longReadVariants
+    priority 5
     bigDataUrl /gbdb/$D/lrSv/gustafson.bb
-    shortLabel 1KG ONT UW 100 SVs
-    longLabel Structural Variants from 1000 Genomes University of Washington ONT - 100 samples (Gustafson et al. 2024)
+    shortLabel 1KG UW ONT SVs
+    longLabel Structural Variants from 100 1000 Genomes samples (University of Washington ONT; Gustafson et al. 2024)
     type bigBed 9 +
     itemRgb on
     visibility hide
     mouseOver <b>Var</b>: $name ($svType)<br><b>SV len</b>: $svLen<br><b>Ins len</b>: $insLen<br><b>AC</b>: $AC<br><b>Samples</b>: $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 noyvertSv
     parent longReadVariants
+    priority 6
     bigDataUrl /gbdb/$D/lrSv/noyvert.bb
-    shortLabel 1KG ONT Boehringer
-    longLabel Structural Variants from 1000 Genomes ONT Boehringer - 888 Individuals (Noyvert et al. 2025)
+    shortLabel 1KG Boehringer ONT SVs
+    longLabel Structural Variants from 888 1000 Genomes samples (Boehringer ONT; Noyvert et al. 2025)
     type bigBed 9 +
     itemRgb on
     visibility hide
     mouseOver <b>Var</b>: ${name} (${svType})<br><b>SV len</b>: ${svLen}<br><b>Ins len</b>: ${insLen}<br><b>AF</b>: ${AF}<br><b>AC</b>: ${AC}/${AN}<br><b>GWAS hits</b>: ${nGwas}
     filterValues.svType DEL,INS,INV,DUP,BND
     filterType.svType multipleListOr
     filterLabel.svType SV Type
     filter.svLen 0:28634664
     filterByRange.svLen on
     filterLabel.svLen SV Length (bp)
     filter.insLen 0:45109
     filterByRange.insLen on
     filterLabel.insLen Insertion Length (bp)
     filter.AC 0:1776
     filterByRange.AC on
@@ -165,34 +166,34 @@
     filter.nGwas 0:11
     filterByRange.nGwas on
     filterLabel.nGwas UK Biobank GWAS Hit Count
     filter.r2Loo 0:1
     filterByRange.r2Loo on
     filterLimits.r2Loo 0:1
     filterLabel.r2Loo Imputation r2 (leave-one-out)
     filter.concordanceLoo 0:1
     filterByRange.concordanceLoo on
     filterLimits.concordanceLoo 0:1
     filterLabel.concordanceLoo Minor Allele Concordance (leave-one-out)
     skipEmptyFields on
 
     track lrSv1kLin
     parent longReadVariants
-    release alpha
+    priority 3
     bigDataUrl /gbdb/$D/lrSv/lin1218.bb
-    shortLabel 1KG Merged 1218 SVs
-    longLabel Structural Variants from 1000 Genomes merged - 1218 individuals (HiFi, ONT & assembly)
+    shortLabel 1KG Lin 1218 SVs
+    longLabel Structural Variants from 1,218 1000 Genomes samples (long-read merge; Lin et al.)
     type bigBed 9 +
     itemRgb on
     visibility hide
     mouseOver <b>Var</b>: $name ($svType)<br><b>SV len</b>: $svLen<br><b>Ins len</b>: $insLen<br><b>AC</b>: $AC/$AN<br><b>AF</b>: $AF<br><b>AF (African)</b>: $afAfr<br><b>AF (European)</b>: $afEur<br><b>Samples</b>: $NS
     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
@@ -216,171 +217,177 @@
     filter.afEur 0:1
     filterByRange.afEur on
     filterLimits.afEur 0:1
     filterLabel.afEur AF European
     filter.afSas 0:1
     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
 
     track aou1kSv
     parent longReadVariants
+    priority 2
     bigDataUrl /gbdb/$D/lrSv/aou1k.bb
     shortLabel AoU 1027 SVs
-    longLabel Structural Variants from 1,027 AoU Individuals (PacBio HiFi Long-read)
+    longLabel Structural Variants from 1,027 All of Us samples (PacBio HiFi)
     type bigBed 9 +
     itemRgb on
     visibility hide
     mouseOver <b>Var</b>: $name ($svType)<br><b>SV len</b>: $svLen<br><b>Ins len</b>: $insLen<br><b>AC (approx)</b>: $AC<br><b>AF (African)</b>: $afAfr<br><b>AF (European)</b>: $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 longReadVariants
+    priority 12
     bigDataUrl /gbdb/$D/lrSv/han945.bb
     shortLabel Han 945 SVs
-    longLabel Structural Variants from 945 Han Chinese (Long-read Sequencing)
+    longLabel Structural Variants from 945 Han Chinese samples (long-read)
     type bigBed 9 +
     itemRgb on
     visibility hide
     mouseOver <b>Var</b>: $name ($svType)<br><b>SV len</b>: $svLen<br><b>Ins len</b>: $insLen<br><b>AF</b>: $alleleFreq<br><b>AC</b>: $AC<br><b>Samples</b>: $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 longReadVariants
+    priority 14
     bigDataUrl /gbdb/$D/lrSv/tommoJp.bb
     shortLabel ToMMo 333 SVs
-    longLabel Structural Variants from 333 Japanese Individuals (ToMMo, 111 Trios)
+    longLabel Structural Variants from 333 Japanese samples (ToMMo, 111 trios)
     type bigBed 9 +
     itemRgb on
     visibility hide
     mouseOver <b>Var</b>: $name ($svType)<br><b>SV len</b>: $svLen<br><b>Ins len</b>: $insLen<br><b>AF</b>: $alleleFreq<br><b>AC</b>: $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 longReadVariants
+    priority 16
     bigDataUrl /gbdb/$D/lrSv/ga4kSv.bb
     shortLabel GA4K 502 SVs
-    longLabel Structural Variants from 502 Children's Mercy GA4K Probands (PacBio HiFi)
+    longLabel Structural Variants from 502 GA4K samples (Children's Mercy, pediatric rare disease; PacBio HiFi)
     type bigBed 9 +
     itemRgb on
     visibility hide
     mouseOver <b>Var</b>: $name ($svType)<br><b>SV len</b>: $svLen<br><b>Ins len</b>: $insLen<br><b>AC (approx)</b>: $AC<br><b>AF</b>: $alleleFreq<br><b>Carriers</b>: $carrierCount/$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 longReadVariants
+    priority 11
     bigDataUrl /gbdb/$D/lrSv/decodeSv.bb
     shortLabel deCODE 3622 SVs
-    longLabel High-confidence Structural Variants from 3,622 Icelanders (deCODE, Oxford Nanopore)
+    longLabel Structural Variants from 3,622 deCODE samples (Icelandic; Oxford Nanopore)
     type bigBed 9 +
     itemRgb on
     visibility hide
     mouseOver <b>Var</b>: $name ($svType)<br><b>SV len</b>: $svLen<br><b>Ins len</b>: $insLen
     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
     skipEmptyFields on
 
     track hprc2v21Sv
     parent longReadVariants
+    priority 7
     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)
+    longLabel Structural Variants from 233 HPRC v2.1 assemblies (minigraph-cactus pangenome graph)
     type bigBed 9 +
     itemRgb on
     visibility hide
     mouseOver <b>Var</b>: $name ($svType)<br><b>SV len</b>: $svLen<br><b>Ins len</b>: $insLen<br><b>AF</b>: $alleleFreq<br><b>AC</b>: $AC/$alleleNumber<br><b>Samples</b>: $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
@@ -424,66 +431,68 @@
     #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 longReadVariants
+    priority 9
     bigDataUrl /gbdb/$D/lrSv/hgsvc2.bb
     shortLabel HGSVC2 32 SVs
-    longLabel Structural Variants from 32 Haplotype-Resolved Genomes (HGSVC2 freeze 4, Ebert 2021)
+    longLabel Structural Variants from 32 HGSVC2 assemblies (freeze 4; Ebert et al. 2021)
     type bigBed 9 +
     itemRgb on
     visibility hide
     mouseOver <b>Var</b>: $name ($svType)<br><b>SV len</b>: $svLen<br><b>Ins len</b>: $insLen<br><b>Samples</b>: $sampleCount<br><b>AC</b>: $AC<br><b>AF</b>: $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 longReadVariants
+    priority 8
     bigDataUrl /gbdb/$D/lrSv/hgsvc3.bb
     shortLabel HGSVC3 65 SVs
-    longLabel Structural Variants from 65 Diverse Samples (HGSVC3 ONT+HIFI)
+    longLabel Structural Variants from 65 HGSVC3 assemblies (diverse ancestry; HiFi + ONT)
     type bigBed 9 +
     itemRgb on
     visibility hide
     mouseOver <b>Var</b>: $name ($svType)<br><b>SV len</b>: $svLen<br><b>Ins len</b>: $insLen<br><b>Samples</b>: $sampleCount<br><b>AC</b>: $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
@@ -537,108 +546,112 @@
     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 longReadVariants
+    priority 15
     bigDataUrl /gbdb/$D/lrSv/apr.bb
     shortLabel Arab APR 53 SVs
-    longLabel Structural Variants from the Arab Pangenome Reference (53 UAE-resident Arab samples)
+    longLabel Structural Variants from 53 Arab Pangenome Reference samples (UAE-resident; HiFi + ONT)
     type bigBed 9 +
     itemRgb on
     visibility hide
     mouseOver <b>Var</b>: $name ($svType)<br><b>SV len</b>: $svLen<br><b>Ins len</b>: $insLen<br><b>AC</b>: $AC/$alleleNumber<br><b>AF</b>: $alleleFreq<br><b>Samples</b>: $numSamples<br><b>Alts</b>: $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 longReadVariants
+    priority 13
     bigDataUrl /gbdb/$D/lrSv/cpc1.bb
     shortLabel CPC 58 SVs
-    longLabel Structural Variants from the Chinese Pangenome Consortium (58 samples, CPC-only)
+    longLabel Structural Variants from 58 Chinese Pangenome Consortium samples (CPC-only; HiFi)
     type bigBed 9 +
     itemRgb on
     visibility hide
     mouseOver <b>Var</b>: $name ($svType)<br><b>SV len</b>: $svLen<br><b>Ins len</b>: $insLen<br><b>AC</b>: $AC/$alleleNumber<br><b>AF</b>: $alleleFreq<br><b>Samples</b>: $numSamples<br><b>Alts</b>: $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 longReadVariants
+    priority 17
     bigDataUrl /gbdb/$D/lrSv/chirmade101.bb
     shortLabel SVatalog 101 SVs
-    longLabel Structural Variants from 101 Long-read WGS (GWAS SVatalog, Chirmade 2026)
+    longLabel Structural Variants from 101 SVatalog samples (cystic fibrosis; Chirmade et al. 2026)
     type bigBed 9 +
     itemRgb on
     visibility hide
     mouseOver <b>Var</b>: $name ($svType)<br><b>SV len</b>: $svLen<br><b>Ins len</b>: $insLen<br><b>Genes</b>: $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
 
     track cardSv
     parent longReadVariants
+    priority 10
     bigDataUrl /gbdb/$D/lrSv/card.bb
     shortLabel CARD 351 SVs
-    longLabel Structural Variants from 351 Brain Samples (NIH CARD Long-read ONT, NABEC + HBCC)
+    longLabel Structural Variants from 351 NIH CARD brain samples (ONT; NABEC + HBCC)
     type bigBed 9 +
     itemRgb on
     visibility hide
     mouseOver <b>Var</b>: ${name} (${svType})<br><b>SV len</b>: ${svLen}<br><b>Ins len</b>: ${insLen}<br><b>AF</b>: ${alleleFreq}<br><b>AC</b>: ${AC} (NABEC ${nabecAc}, HBCC ${hbccAc})
     filterValues.svType DEL,INS,INV,DUP
     filterType.svType multipleListOr
     filterLabel.svType SV Type
     filter.svLen 0:30282742
     filterByRange.svLen on
     filterLabel.svLen SV Length
     filter.insLen 0:92867161
     filterByRange.insLen on
     filterLabel.insLen Insertion Length
     filter.AC 0:702
     filterByRange.AC on