A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv938921



Internal ID16232877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:23829044..23882207hg38UCSC Ensembl
Innerchr20:23809681..23862844hg19UCSC Ensembl
Innerchr20:23757681..23810844hg18UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg3853164
hg1953164
hg1853164
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv585730
Supporting Variants
Samples
Known GenesCST5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv938921
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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