1bd2b1f3f86df6284bc45e1075fe011d215d1d78
abenetpa
  Thu May 21 09:19:55 2020 -0700
correct typos as in refs #25424

diff --git src/hg/makeDb/trackDb/human/dbVarConflict.html src/hg/makeDb/trackDb/human/dbVarConflict.html
index 917063d..11e5a5c 100644
--- src/hg/makeDb/trackDb/human/dbVarConflict.html
+++ src/hg/makeDb/trackDb/human/dbVarConflict.html
@@ -1,66 +1,66 @@
 <h2>Description</h2>
 The track <b>NCBI dbVar Curated Common SVs: Conflicts with Pathogenic</b> highlights loci where
 common copy number variants from
 <a target=_blank href="https://www.ncbi.nlm.nih.gov/dbvar/studies/nstd186/">nstd186 (NCBI Curated 
 Common Structural Variants)</a> overlap with structural Variants with clinical assertions,
 submitted to ClinVar by external labs <a target=_blank 
 href="https://www.ncbi.nlm.nih.gov/dbvar/content/var_summary/#nstd102">(Clinical Structural 
 Variants - nstd102)</a>.
 </p>
 
 <p>
 <em>Overlap</em> in the track refers to reciprocal overlap between variants in the <b><em>common</em>
 (NCBI Curated Common Structural Variants)</b> versus <b><em>clinical</em> (ClinVar Long Variants)</b>
 tracks. Reciprocal overlap values can be anywhere from 10% to 100%.
 </p>
 
 <p>
 For more information on the number of variant calls and latest statistics for nstd186 see
 <a target=_blank href="https://www.ncbi.nlm.nih.gov/dbvar/content/common_summary/">Summary of nstd186</a>
 (NCBI Curated Common Structural Variants).
 </p>
 
 <h2>Display Conventions and Configuration</h2>
 Items in all subtracks follow the same conventions: items are shaded according to variant type.
 <b><font color="red">Red</font></b> for copy number loss or deletion, <b><font color="blue">blue</font></b>
 for copy number gain or duplication and <b><font color="#662180">violet</font></b> for copy number variation.
 Mouseover on items indicates Allele Frequencies (AF).
 </p>
 
 <p> 
 All tracks can be filtered according to the <b>variant lenth</b> and <b>type of variant</b>. The
 <b>variant overlap</b> filter defines four bins within that range from which the user can choose.
 </p>
  
 
-<h2>Data Acces</h2>
+<h2>Data Access</h2>
 The raw data can be explored interactively with the 
 <a href="https://genome.ucsc.edu/cgi-bin/hgTables">Table Browser</a>, or the 
 <a href="https://genome.ucsc.edu/cgi-bin/hgIntegrator">Data Integrator</a>. For automated analysis,
 the data may be queried from our
 <a href="https://genome.ucsc.edu/goldenPath/help/api.html">REST API</a>.
 </p>
 
 <p>
 The data can also be found directly from the dbVar nstd186 
 <a target=_blank href="https://www.ncbi.nlm.nih.gov/dbvar/content/common_summary/#data_access">data access</a>.
 For questions about dbVar track data, please contact <em>dbvar@ncbi.nlm.nih.gov</em>.
 </p>
 
 <h2>Credits</h2>
 Thanks to the dbVAR team at NCBI, especially Timothy Hefferon for technical coordination and consultation,
-and to Christopher Lee, Anna Benet-Pages, and Maximilian Haeussler of the Genome Browser team for 
-engineering the track display.
+and to Christopher Lee, Anna Benet-Pages, and Maximilian Haeussler of the Genome 
+Browser team for engineering the track display.
 </p>
  
 <h2>References</h2>
 <p>
 Lappalainen I, Lopez J, Skipper L, Hefferon T, Spalding JD, Garner J, Chen C, Maguire M, Corbett M,
 Zhou G <em>et al</em>.
 <a href="https://academic.oup.com/nar/article-lookup/doi/10.1093/nar/gks1213" target="_blank">
 DbVar and DGVa: public archives for genomic structural variation</a>.
 <em>Nucleic Acids Res</em>. 2013 Jan;41(Database issue):D936-41.
 PMID: <a href="https://www.ncbi.nlm.nih.gov/pubmed/23193291" target="_blank">23193291</a>; PMC: <a
 href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3531204/" target="_blank">PMC3531204</a>
 </p>