af24c692f12ca0c3fcbf639e63040e61cfb684a5
max
  Sat Jul 18 00:17:03 2026 -0700
small lrsv docs changes

diff --git src/hg/makeDb/trackDb/human/lrSv.html src/hg/makeDb/trackDb/human/lrSv.html
index e1873d4fbb0..9110e43be88 100644
--- src/hg/makeDb/trackDb/human/lrSv.html
+++ src/hg/makeDb/trackDb/human/lrSv.html
@@ -341,45 +341,45 @@
 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=chirmade101Sv">SVatalog 101 SVs</a></h3>
+<h3><a href="hgTrackUi?g=chirmade101Sv">SVatalog 101 SVs - Cystic Fibrosis</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
 responses to CFTR modulator therapies (most participants are F508del
 homozygotes or F508del / minimal-function compound heterozygotes; a smaller
 number carry rare nonsense or missense CFTR mutations). ~87k SVs
 (deletions, insertions, duplications, inversions and complex events)
 annotated with gene overlaps, ClinGen / gnomAD constraint scores,
 OMIM / ClinVar / DGV / Decipher regional annotations.
 </p>
 
-<h3><a href="hgTrackUi?g=cardSv">NIH CARD 351 SVs</a></h3>
+<h3><a href="hgTrackUi?g=cardSv">NIH CARD 351 SVs - Alzheimer's and related dementias</a></h3>
 <p>
 Structural variants from Oxford Nanopore long-read sequencing of post-mortem
 brain tissue (prefrontal cortex) from 351 neurologically normal individuals,
 generated by the NIH Center for Alzheimer's and Related Dementias (NIH CARD)
 Long-Read Initiative (Billingsley et al. 2024). The cohort combines 205
 European-ancestry samples (North American Brain Expression Consortium, NABEC)
 and 146 African / African-admixed samples (NIMH Human Brain Collection Core,
 HBCC). ~229k SVs (insertions, deletions, inversions) with per-cohort carrier
 counts and allele frequencies.
 </p>
 
 <h3><a href="hgTrackUi?g=noyvertSv">Noyvert 888 SVs</a></h3>
 <p>
 Structural variants from Oxford Nanopore long-read sequencing of 888
 individuals from the 1000 Genomes Project, spanning five ancestry groups