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

diff --git src/hg/makeDb/trackDb/human/dbVarCurated.html src/hg/makeDb/trackDb/human/dbVarCurated.html
index 232f461..29c956c 100644
--- src/hg/makeDb/trackDb/human/dbVarCurated.html
+++ src/hg/makeDb/trackDb/human/dbVarCurated.html
@@ -1,85 +1,85 @@
 <h2>Description</h2>
 <p>
 The tracks listed here contain data from the
 <a target=_blank href="https://www.ncbi.nlm.nih.gov/dbvar/content/var_summary/#nstd186">
 nstd186 (NCBI Curated Common Structural Variants)</a> study. This is a collection of structural
 variants (SV) originally submitted to dbVar which are part of a study with at least 100 samples and
 have an allele frequency of &gt;=0.01 in at least one population. The complete dataset is imported
 from these common-population studies:
 </p>
 
 <p>
 <b>gnomAD Structural Variants</b>
 <a target=_blank href="https://www.ncbi.nlm.nih.gov/dbvar/studies/nstd166/">(nstd166)</a>:
  Catalog of SVs detected from the sequencing of the complete genome of 10,847 unrelated
 individuals from the GnomAD v2.1 release.</p>
 <p>
 <b>1000 Genomes Consortium Phase 3 Integrated SV</b>
 <a target=_blank href="https://www.ncbi.nlm.nih.gov/dbvar/studies/estd219/">(estd219)</a>:
  Structural variants of the 1000 Genomes project Phase 3 as reported in a separate article
 specifically dedicated to the analysis of SVs. Many of these data are identical to those reported
 in the <a target=_blank 
 href="https://www.ncbi.nlm.nih.gov/dbvar/studies/estd214/">estd214</a> study.</p>
 <p>
 <b>DECIPHER Common CNVs</b>
 <a href="https://www.ncbi.nlm.nih.gov/dbvar/studies/nstd183/">(nstd183)</a>:
 Consensus set of common population CNVs selected from high-resolution controls sets where frequency
 information is available.
 </p>
 
 <p>
 There are two tracks in this collection:
 <ul>
 <li><a href="/cgi-bin/hgTrackUi?hgsid=395092309_WCeXo2V0Ug6yJ1KducDbjPkMSade&c=chr1&g=dbVar_common">
 <b>NCBI dbVar Curated Common Structural Variants (dbVar Common SV)</b></a>: Shows copy number
 variants calls (variants &gt;=50 nucleotides) from the <a target=_blank 
 href="https://www.ncbi.nlm.nih.gov/dbvar/studies/nstd186/">nstd186</a> study.</li>
 <li><a href="/cgi-bin/hgTrackUi?hgsid=395092309_WCeXo2V0Ug6yJ1KducDbjPkMSade&c=chr1&g=dbVar_conflict">
 <b>NCBI dbVar Curated Conflict Variants (dbVar Conflict SV)</b></a>: Shows copy number
 variants from <a target=_blank href="https://www.ncbi.nlm.nih.gov/dbvar/studies/nstd186/">nstd186</a>
 (NCBI Curated Common Structural Variants) that overlap with
 <a target=_blank href="https://www.ncbi.nlm.nih.gov/dbvar/studies/nstd102/">nstd102</a> (Clinical
 Structural Variants).</li>
 </ul>
 </p>
 
 <h2>Display Conventions</h2>
 <p>
 These tracks are multi-view composite tracks that contain multiple data types (views). Each view
 within a track has separate display controls, as described
 <a href="https://genome.ucsc.edu/goldenPath/help/multiView.html">here</a>. Some dbVar tracks
 contain multiple subtracks, corresponding to subsets of data. If a track contains many subtracks,
 only some subtracks will be displayed by default. The user can select which subtracks are displayed
 via the display controls on the track details page.
 </p>
 
-<h2>Data Acces</h2>
+<h2>Data Access</h2>
 <p>
 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 
+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>