46fb2ffff6cdf0a620ff9ab18fc86d0f7f1d7806
jnavarr5
  Wed Sep 24 17:30:46 2025 -0700
Staging the CoLoRSdb track for hg38 and hs1, refs #34120

diff --git src/hg/makeDb/trackDb/human/structuralVariants.html src/hg/makeDb/trackDb/human/structuralVariants.html
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+<h2>Description</h2>
+<p>
+The tracks listed here contain structural variants using long-read sequencing technologies.</p>
+<ul>
+    <li>CoLoRSdb Small variants: small genetic variants (single nucleotide polymorphisms and short
+        insertions and deletions) called with DeepVariant and merged with GLnexus/bcftools.</li>
+    <li>CoLoRdb Structural variants: structural variants (insertions, deletions, and inversions)
+        discovered with pbsv and merged across samples using Jasmine.</li>
+</ul>
+
+<h2>Display conventions</h2>
+<p>
+Hover over the feature to see more information, explained on teh track details page of the
+particular track or when clicking onto the feature.</p>
+
+<h2>Credits</h2>
+<p>
+For data provenance, access and descriptions, please click the documentation via the link above.
+</p>