6b0d68657267f1e02c47d4224ea62446bbbb2ba0
max
  Fri May 22 06:55:52 2026 -0700
small non-AI changes to the html docs pages of the long-read SV tracks

diff --git src/hg/makeDb/trackDb/human/lrSv.html src/hg/makeDb/trackDb/human/lrSv.html
index ebf9c5bdf1f..4a6736c66a4 100644
--- src/hg/makeDb/trackDb/human/lrSv.html
+++ src/hg/makeDb/trackDb/human/lrSv.html
@@ -10,31 +10,31 @@
 <h3>Available Datasets</h3>
 <p>
 SV length statistics (min / median / max) are computed from the <tt>svLen</tt>
 field of each track, in base pairs. Some tracks include sites with
 <tt>svLen=0</tt> (complex events where the reference and alternate alleles
 differ in sequence but not in length).
 </p>
 <p>
 For short-read structural-variant comparators (CCDG 17,795, 1KG 3202,
 ToMMo 48K CNV) see the companion
 <a href="hgTrackUi?g=srSv">Short-read SVs</a> supertrack.
 </p>
 <p>
 Polymorphic <b>Mobile Element Insertions</b> (Alu, L1, SVA, HERVK,
 snRNA) called from HGSVC3 long-read assemblies are released as a
-separate track collection &mdash; see the
+separate track collection; see the
 <a href="hgTrackUi?g=mei">Mobile Insertions</a> tracks. Those MEIs are
 the insertions identified in the 65 HGSVC3 samples relative to the
 reference, available on both GRCh38/hg38 and T2T-CHM13/hs1.
 </p>
 <table class="stdTbl">
 <tr>
   <th>Dataset</th>
   <th>N samples</th>
   <th>Cohort / disease</th>
   <th>Disease cases</th>
   <th>Coverage</th>
   <th>SV count</th>
   <th>Min</th>
   <th>Median</th>
   <th>Max</th>