e6bcec351aa8f5bc7218e8862e15c149aadb3479 lrnassar Fri Jul 10 12:18:40 2026 -0700 lrSv: complete the longReadVariants rename - reparent subtracks and update refs. refs #36258 Completes the previous rename commit (which carried only the colorsDbLegacy file moves). Renames "track lrSv" to "track longReadVariants" in lrSv.ra (adds "html lrSv" to keep the existing description page), reparents all subtracks plus the merged lrSvAll and its lrSvMergeAll.py generator, and updates the hs1 override, relatedTracks.ra, and the mei/meiHgsvc3/srSv/lrSvAll cross-links. Retitles the retired colorsDbLegacy track and reparents its subtracks. Only the internal track name changes; subtrack names, /gbdb/$D/lrSv/ data paths, and the lrSv.ra filename are unchanged. diff --git src/hg/makeDb/trackDb/human/lrSvAll.html src/hg/makeDb/trackDb/human/lrSvAll.html index 1b97f6518c6..b12c1a8b655 100644 --- src/hg/makeDb/trackDb/human/lrSvAll.html +++ src/hg/makeDb/trackDb/human/lrSvAll.html @@ -1,19 +1,19 @@

Description

This track combines the structural-variant (SV) callsets from the individual -subtracks of the Long-read SVs supertrack into a +subtracks of the Long-read SVs supertrack into a single, position-merged overview. Each item is an SV locus seen in one or more of the contributing long-read databases. For every merged locus the track records which databases report it, the summed allele count across those databases, and the range of allele frequencies observed, making it useful for quickly seeing how widely an SV has been reported across cohorts.

This is a summary view. For cohort-specific genotypes, per-population allele frequencies, and dataset-specific annotations, use the individual subtracks of the supertrack. The merge includes the released long-read callsets only; preliminary or unpublished subtracks (e.g. the Kim PD brain, 1000 Genomes linear, and HPRC Jasmine sets) are not part of this merged track.

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