A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5027909



Internal ID8217235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:61715436..61740822hg38UCSC Ensembl
Innerchr20:60290492..60315878hg19UCSC Ensembl
Innerchr20:59723887..59749273hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3825387
hg1925387
hg1825387
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2421637
Supporting Variants
SamplesNA20847
Known GenesCDH4
MethodSNP array
AnalysisTo assess copy number variation we merged and analysed the probe level intensity data from both the Affymetrix and Illumina arrays.
PlatformNot specified
Comments
ReferenceAltshuler_et_al_2010
Pubmed ID20811451
Accession Number(s)essv5027909
Frequency
Sample Size1184
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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