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

diff --git src/hg/makeDb/trackDb/human/dbVarCommon.html src/hg/makeDb/trackDb/human/dbVarCommon.html
index d2f88c4..a386a35 100644
--- src/hg/makeDb/trackDb/human/dbVarCommon.html
+++ src/hg/makeDb/trackDb/human/dbVarCommon.html
@@ -49,44 +49,44 @@
 <a href="https://www.ncbi.nlm.nih.gov/dbvar/studies/nstd186">Variants</a> with AF &gt;= 0.01 from 
 1000 Genomes Consortium Phase 3 Integrated SV.</li>
 <li><b>NCBI Curated Common SVs: all populations from DECIPHER -</b>
 <a href="https://www.ncbi.nlm.nih.gov/dbvar/studies/nstd186">Variants</a> with AF &gt;= 0.01 from 
 DECIPHER Consensus CNVs.</li>
 </ul>
 </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). All tracks can be filtered according to the Variant Size and Variant Type.
 
-<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>.
 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>
 <p>
 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 Genom
-Browser team for engineering the track display. 
+consultation, 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>