65091fe6f6487c23d650a144e947fc1c582d3f40
max
Tue Apr 21 02:16:16 2026 -0700
abelSv: move under lrSv supertrack as short-read comparison subtrack
Move the Abel et al. 2020 CCDG 17,795-genome SV callset from a
top-level hg38 track to a subtrack of the lrSv supertrack (parallel
to onekg3202Sr) and relabel shortLabel/longLabel to flag Illumina
short-read provenance. The same bigBed is now visible on hg38 in
the long-read SV browsing context. Also:
- Clarify abelSv.html variant counts: 738,624 upstream unique SVs
across both callsets, 737,998 after B37->hg38 liftOver (626
unmapped). B38=458,106, B37lift=279,892.
- lrSv.html: fix triple-slash https:/// in the Ebert et al. Science
reference URL.
- bigBed.html: add closing on the extra-fields pipe-separator
bullet and tighten a comma in the same sentence.
refs #36258, refs #37376
diff --git src/hg/makeDb/trackDb/human/lrSv.ra src/hg/makeDb/trackDb/human/lrSv.ra
index f51bf6bfca1..808454bdf4b 100644
--- src/hg/makeDb/trackDb/human/lrSv.ra
+++ src/hg/makeDb/trackDb/human/lrSv.ra
@@ -43,30 +43,69 @@
filterType.insType multipleListOr
filterLabel.insType Insertion/Deletion Type
filterValues.family Alu,HERVK,L1,LTR5_Hs,SVA
filterType.family multipleListOr
filterLabel.family Transposon Family
filterByRange.svLen on
filterLabel.svLen SV Length
filterByRange.alleleFreq on
filterLimits.alleleFreq 0:1
filterLabel.alleleFreq Allele Frequency
filterByRange.alleleCount on
filterLabel.alleleCount Allele Count
skipEmptyFields on
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 $name ($svType) len=$svLength AF=$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.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)
+ 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 $name ($svType) len=$svLen AF=$alleleFreq AC=$alleleCount/$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