A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1151404



Internal ID15872690
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 loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv586441
Supporting Variants
SamplesHGDP00017
Known GenesCDH4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1151404
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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