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 Var: ${name} (${svType})
SV len: ${svLen}
Ins len: ${insLen}
AF: ${AF}
AC: ${AC}/${AN}
GWAS hits: ${nGwas}
+ filterValues.svType DEL,INS,INV,DUP,BND
+ filterType.svType multipleListOr
+ filterLabel.svType SV Type
+ filter.svLen 0:28634664
+ filterByRange.svLen on
+ filterLabel.svLen SV Length (bp)
+ filter.insLen 0:45109
+ filterByRange.insLen on
+ filterLabel.insLen Insertion Length (bp)
+ filter.AC 0:1776
+ filterByRange.AC on
+ filterLabel.AC Allele Count (approx)
+ filter.AF 0:1
+ filterByRange.AF on
+ filterLimits.AF 0:1
+ filterLabel.AF Allele Frequency
+ filter.afAfr 0:1
+ filterByRange.afAfr on
+ filterLimits.afAfr 0:1
+ filterLabel.afAfr AF African
+ filter.afAmr 0:1
+ filterByRange.afAmr on
+ filterLimits.afAmr 0:1
+ filterLabel.afAmr AF Admixed American
+ filter.afEas 0:1
+ filterByRange.afEas on
+ filterLimits.afEas 0:1
+ filterLabel.afEas AF East Asian
+ filter.afEur 0:1
+ filterByRange.afEur on
+ filterLimits.afEur 0:1
+ filterLabel.afEur AF European
+ filter.afSas 0:1
+ filterByRange.afSas on
+ filterLimits.afSas 0:1
+ filterLabel.afSas AF South Asian
+ filter.nGwas 0:11
+ filterByRange.nGwas on
+ filterLabel.nGwas UK Biobank GWAS Hit Count
+ filter.r2Ukb 0:1
+ filterByRange.r2Ukb on
+ filterLimits.r2Ukb 0:1
+ filterLabel.r2Ukb Imputation r2 (UK Biobank)
+ skipEmptyFields on
+
# NOT FOR RELEASE: data received from Eichler lab via email, not yet published.
# Do not add to lrSvAll merged track until a preprint or paper is available.
track lrSv1kLin
parent longReadVariants
release alpha
bigDataUrl /gbdb/$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 Var: $name ($svType)
SV len: $svLen
Ins len: $insLen
AC: $AC/$AN
AF: $AF
AF (African): $afAfr
AF (European): $afEur
Samples: $NS
filterValues.svType DEL,INS
filterType.svType multipleListOr
filterLabel.svType SV Type