ebc68f5e6151d7f361887c0027bb4cd8776c277e
kuhn
  Mon Jul 27 12:11:37 2020 -0700
fixing typo in last fix

diff --git src/hg/makeDb/trackDb/human/clinvar.html src/hg/makeDb/trackDb/human/clinvar.html
index 4d76664..cc04865 100644
--- src/hg/makeDb/trackDb/human/clinvar.html
+++ src/hg/makeDb/trackDb/human/clinvar.html
@@ -29,31 +29,31 @@
 <h2>Display Conventions and Configuration</h2>
 
 <p>
 Genomic locations of ClinVar variants are labeled with the ClinVar variant
 descriptions. All information related to each is variant is shown on that
 variant's details page.  Leave the mouse over a feature for more than 2 seconds
 to show the clinical significance of a variant.
 </p>
 
 <p>The track is divided into two subtracks, one for copy number variants (CNVs), which are all 
 variants longer than 50bp, and a second track for shorter substitutions and indels.</p>
 
 <p>
 Until October 2017, all variants with the ClinVar types copy number gain/loss
 and DbVar "nsv" accessions were put in the CNV category.  Due
-to the ClinVar type lon longer capturing this information, anything longer
+to the ClinVar type no longer capturing this information, anything longer
 than 50bp is now considered a CNV.</p>
 
 <p>
 Entries in the ClinVar CNV track are colored
 <b><font color="red">red for loss</font></b> and
 <B><font color="blue">blue for gain</font></b>.
 </p>
 
 <p>
 Entries in the ClinVar short variants track are shaded by clinical annotation:
 <b><font color="red">red for pathogenic</font></b>,
 <B><font color="#888">dark grey for uncertain significance or not provided</font></b> and
 <B><font color="#000088">dark blue for variant of uncertain significance</font></b> and
 <B><font color="#ADD8E6">light blue for conflicting</font></b> and
 <B><font color="green">green for benign</font></b>.