2e0addd016cfcbf61485b90d8980a8d75be622c2 lrnassar Sun Jun 14 00:10:06 2026 -0700 lrSv: sync description-page counts to the deduped data; drop Kim PD from the supertrack page. refs #36258 After the QA dedup, update the SV counts cited on the description pages to the unique (post-dedup) totals for the tracks served, while leaving the upstream release/paper counts in the Methods sections: decodeSv 133,886 -> 119,453 displayed gustafsonSv 113,696 -> 113,159 displayed chirmade101 87,183 -> 87,068 displayed aou1k 541,049 -> 540,155 displayed hprc2v21Sv 596,063 -> 549,649 (hg38) and 608,435 -> 541,176 (hs1), throughout (no upstream publication), incl. recomputed nested-snarl counts lrSv.html: update the Available Datasets table count cells to match, set the lrSvAll merged cell to 2,317,508 (post Kim PD removal), and remove the Kim PD Brain row, blurb and reference from the supertrack page (the track is staged on dev/alpha only, kept out of the merge and the description, and is not released). diff --git src/hg/makeDb/trackDb/human/chirmade101Sv.html src/hg/makeDb/trackDb/human/chirmade101Sv.html index 1ffe94e15a3..dc35b075c66 100644 --- src/hg/makeDb/trackDb/human/chirmade101Sv.html +++ src/hg/makeDb/trackDb/human/chirmade101Sv.html @@ -1,28 +1,29 @@ <h2>Description</h2> <p> This track shows structural variants (SVs) identified by long-read whole-genome sequencing of 101 individuals, released together with the <a href="https://svatalog.research.sickkids.ca/" target="_blank">GWAS SVatalog</a> web tool described in Chirmade et al. 2026. GWAS SVatalog computes and visualizes linkage disequilibrium between these SVs and GWAS-associated SNPs so that investigators can assess whether a SNP association signal may be tagging an underlying SV. </p> <p> -The table contains 87,183 SVs (42,435 deletions, 41,734 insertions, -1,394 duplications, 912 inversions, 708 complex events). Each SV is +The table contains 87,068 SVs (42,435 deletions, 41,619 insertions, +1,394 duplications, 912 inversions, 708 complex events; byte-identical +duplicate records have been removed). Each SV is annotated with gene overlaps, GC content, repeat context, ClinGen haploinsufficiency / triplosensitivity scores, gnomAD per-gene constraint metrics (pLI, LOEUF, missense O/E), OMIM phenotype associations, ClinVar variant IDs, and overlaps with DGV, Decipher and ClinGen regional annotations. </p> <h2>Display Conventions and Configuration</h2> <p> Items are colored by SV type: <ul> <li><span style="color: rgb(200,0,0);">Deletions (del)</span> - red</li> <li><span style="color: rgb(0,0,200);">Insertions (ins)</span> - blue</li> <li><span style="color: rgb(0,160,0);">Duplications (dup)</span> - green</li> <li><span style="color: rgb(230,140,0);">Inversions (inv)</span> - orange</li>