A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv938988



Internal ID16232944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:25806460..25967691hg38UCSC Ensembl
Innerchr20:25787096..25948327hg19UCSC Ensembl
Innerchr20:25735096..25896327hg18UCSC Ensembl
Cytoband20p11.1
Allele length
AssemblyAllele length
hg38161232
hg19161232
hg18161232
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv585759
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv938988
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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