3bf9e1a841206d3bf5902e06791ef5be2dbdbd39 max Fri Jul 17 09:09:47 2026 -0700 lrSv: add Noyvert multi-ancestry long-read SV subtrack (noyvertSv) #Preview2 week - bugs introduced now will need a build patch to fix 888 Oxford Nanopore 1000 Genomes genomes, Sniffles2 v2.0.7, 107,445 SVs with per-superpopulation allele frequencies, imputation-accuracy metrics and UK Biobank SV-WAS associations. Converter approximates AC/AN from AF and the genotype missing rate (source has no allele count), stores BND mate breakends, and follows the shared lrSv svType/svLen/insLen/AC field convention so the container-level filters apply. refs #36258 diff --git src/hg/makeDb/trackDb/human/lrSv.ra src/hg/makeDb/trackDb/human/lrSv.ra index bfb4f3ba0be..ee7ba629c4a 100644 --- src/hg/makeDb/trackDb/human/lrSv.ra +++ src/hg/makeDb/trackDb/human/lrSv.ra @@ -533,30 +533,84 @@ filterLabel.insLen Insertion Length filter.AC 1:351 filterByRange.AC on filterLabel.AC Carrier Count filter.alleleFreq 0:1 filterByRange.alleleFreq on filterLimits.alleleFreq 0:1 filterLabel.alleleFreq Allele Frequency filter.nabecCount 0:205 filterByRange.nabecCount on filterLabel.nabecCount NABEC Carriers (European ancestry) filter.hbccCount 0:146 filterByRange.hbccCount on filterLabel.hbccCount HBCC Carriers (African/African-admixed ancestry) + track noyvertSv + parent longReadVariants + bigDataUrl /gbdb/$D/lrSv/noyvert.bb + shortLabel Noyvert 888 SVs + longLabel Structural Variants from 888 Multi-ancestry Individuals (Oxford Nanopore, 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>: ${nGwas} + filterValues.svType DEL,INS,INV,DUP,BND + filterType.svType multipleListOr + filterLabel.svType SV Type + filter.svLen 0:28634664 + filterByRange.svLen on + filterLabel.svLen SV Length (bp) + filter.insLen 0:45109 + filterByRange.insLen on + filterLabel.insLen Insertion Length (bp) + filter.AC 0:1776 + filterByRange.AC on + filterLabel.AC Allele Count (approx) + filter.AF 0:1 + filterByRange.AF on + filterLimits.AF 0:1 + filterLabel.AF Allele Frequency + filter.afAfr 0:1 + filterByRange.afAfr on + filterLimits.afAfr 0:1 + filterLabel.afAfr AF African + filter.afAmr 0:1 + filterByRange.afAmr on + filterLimits.afAmr 0:1 + filterLabel.afAmr AF Admixed American + filter.afEas 0:1 + filterByRange.afEas on + filterLimits.afEas 0:1 + filterLabel.afEas AF East Asian + filter.afEur 0:1 + filterByRange.afEur on + filterLimits.afEur 0:1 + filterLabel.afEur AF European + filter.afSas 0:1 + filterByRange.afSas on + filterLimits.afSas 0:1 + filterLabel.afSas AF South Asian + filter.nGwas 0:11 + filterByRange.nGwas on + filterLabel.nGwas UK Biobank GWAS Hit Count + filter.r2Ukb 0:1 + filterByRange.r2Ukb on + filterLimits.r2Ukb 0:1 + filterLabel.r2Ukb Imputation r2 (UK Biobank) + skipEmptyFields on + # NOT FOR RELEASE: data received from Eichler lab via email, not yet published. # Do not add to lrSvAll merged track until a preprint or paper is available. track lrSv1kLin parent longReadVariants release alpha bigDataUrl /gbdb/$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 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