c7e0e71c357fa4630ac2ee1fb0520a32d408a1e2
lrnassar
  Sat Jun 13 09:33:29 2026 -0700
lrSv QA round 2: alpha-gate unpublished subtracks, trim labels, fill dataset blurbs. refs #36258

Add "release alpha" to hprc2JasmineSv and lrSv1kLin so the two unpublished /
do-not-release-yet subtracks stay on dev/alpha and do not graduate with the
supertrack (both are already excluded from the lrSvAll merge via databases.tsv).
Trim three longLabels to the 85-char limit: hprc2v21Sv, hprc2JasmineSv, and
lrSv1kLin.
lrSv.html: add the missing "Available Datasets" prose blurbs for Arab APR and
CPC so all 15 datasets have a paragraph (was table-row-only).

diff --git src/hg/makeDb/trackDb/human/lrSv.html src/hg/makeDb/trackDb/human/lrSv.html
index 803d8904725..4b396be3b91 100644
--- src/hg/makeDb/trackDb/human/lrSv.html
+++ src/hg/makeDb/trackDb/human/lrSv.html
@@ -312,30 +312,49 @@
 inversions) called from phased de novo assemblies with PAV, with
 per-variant 1000 Genomes population allele frequencies (insertions and
 deletions) and rich structural/gene annotations. An earlier HGSVC release
 complementary to <a href="hgTrackUi?g=hgsvc3Sv">HGSVC3</a>.
 </p>
 
 <h3><a href="hgTrackUi?g=hgsvc3Sv">HGSVC3 65 SVs</a></h3>
 <p>
 Structural variants from 65 diverse individuals sequenced and de novo
 assembled by the Human Genome Structural Variation Consortium phase 3
 (HGSVC3). ~177k haplotype-resolved SVs (deletions, insertions and
 inversions) called with PAV and cross-validated with ten additional callers,
 with per-site carrier haplotype lists and structural annotations.
 </p>
 
+<h3><a href="hgTrackUi?g=aprSv">Arab APR 53 SVs</a></h3>
+<p>
+Structural variants from the Arab Pangenome Reference (APR), a
+haplotype-resolved pangenome graph built from 53 UAE-resident Arab individuals
+drawn from eight countries (PacBio HiFi + ultralong ONT + Hi-C; Nassir et al.
+2025). ~73k SVs on hg38 (deletions, insertions, complex and mixed snarls),
+lifted from the native T2T-CHM13 assembly; the hs1 track uses the native
+coordinates.
+</p>
+
+<h3><a href="hgTrackUi?g=cpc1Sv">CPC 58 SVs</a></h3>
+<p>
+Structural variants from the Chinese Pangenome Consortium (CPC), 58 samples
+spanning 36 minority ethnic groups (PacBio HiFi pangenome graph; Gao et al.
+2023). This track shows the CPC contribution to the joint CPC+HPRC graph with
+HPRC-specific SVs removed. ~36k SVs on hg38 (deletions, insertions and mixed
+snarls), lifted from the native T2T-CHM13 assembly; the hs1 track is native.
+</p>
+
 <h3><a href="hgTrackUi?g=kwanhoSv">Kim PD Brain SVs</a></h3>
 <p>
 Structural variants from 100 post-mortem brain samples (Parkinson's disease,
 incidental Lewy body disease, and healthy controls) sequenced with PacBio
 HiFi long reads. ~75k high-confidence SVs (deletions, insertions,
 duplications, inversions) with per-cohort allele frequencies and
 case-control carrier-rate differentials, from Kim et al. 2026.
 </p>
 
 <h3><a href="hgTrackUi?g=chirmade101Sv">SVatalog 101 SVs</a></h3>
 <p>
 Structural variants from 101 long-read whole-genome sequences released
 alongside the GWAS SVatalog tool (Chirmade et al. 2026). The samples come
 from the CF Canada-Sick Kids Program in Individual CF Therapy (CFIT), a
 cystic-fibrosis (CF) patient cohort assembled to model patient-specific