9a63ecfed718d4ad0b2c5212c7ad8844c9d23531
lrnassar
  Mon Jun 29 14:21:07 2026 -0700
lrSv: add GitHub source links (makedoc, scripts, trackDb.ra) to all description pages. refs #36258

Per the updated qa-track standard, link the track's UCSC source artifacts on
github.com/ucscGenomeBrowser/kent from every lrSv description page:
- Add the missing links to the lrSv supertrack page and colorsDbSv.
- Backfill the trackDb.ra link (third artifact) across the subtrack pages that
already linked the makedoc + scripts dir.
lrSv1kLin is left as its placeholder (staged, not released).

diff --git src/hg/makeDb/trackDb/human/hprc2v21Sv.html src/hg/makeDb/trackDb/human/hprc2v21Sv.html
index 196796a19a3..724e1b9956c 100644
--- src/hg/makeDb/trackDb/human/hprc2v21Sv.html
+++ src/hg/makeDb/trackDb/human/hprc2v21Sv.html
@@ -62,31 +62,32 @@
 is shorter. At this size no balanced, equal-length substitutions came up,
 and the files carry no inversion calls, so the track has only insertions and
 deletions. On hg38, 549,649 alleles were kept (40,678 at nested snarl
 levels); on hs1, 541,176 (70,200 nested), after removing byte-identical
 duplicate records. Because these files are not broken
 down into atomic indels, one bubble can appear as a single large allele
 rather than several small ones, so the counts are not comparable to a
 wave-decomposed callset. Allele counts, frequencies and sample counts come
 straight from the VCF.
 </p>
 <p>
 The conversion script and autoSql schema are in
 <a href="https://github.com/ucscGenomeBrowser/kent/tree/master/src/hg/makeDb/scripts/lrSv" target="_blank">
 makeDb/scripts/lrSv</a> and the build steps are in the makeDoc at
 <a href="https://github.com/ucscGenomeBrowser/kent/blob/master/src/hg/makeDb/doc/hg38/lrSv.txt" target="_blank">
-doc/hg38/lrSv.txt</a>.
+doc/hg38/lrSv.txt</a>, and the track configuration is in
+<a href="https://github.com/ucscGenomeBrowser/kent/blob/master/src/hg/makeDb/trackDb/human/lrSv.ra" target="_blank">trackDb/human/lrSv.ra</a>.
 </p>
 
 <h2>Data Access</h2>
 <p>
 The data can be explored interactively in table format with the
 <a href="hgTables">Table Browser</a> or the
 <a href="hgIntegrator">Data Integrator</a>, and read programmatically
 through our <a href="https://api.genome.ucsc.edu">API</a>,
 track=<i>hprc2v21Sv</i>. For automated download and analysis the variants
 are in a bigBed file on our download server, one per assembly:
 <a href="http://hgdownload.soe.ucsc.edu/gbdb/hg38/lrSv/hprc2v21.bb" target="_blank">
 hg38</a> and
 <a href="http://hgdownload.soe.ucsc.edu/gbdb/hs1/lrSv/hprc2v21.bb" target="_blank">
 hs1</a>. You can pull out one region or the whole set with
 <tt>bigBedToBed</tt>, for example