A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv938985



Internal ID16232941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:25805665..25967458hg38UCSC Ensembl
Innerchr20:25786301..25948094hg19UCSC Ensembl
Innerchr20:25734301..25896094hg18UCSC Ensembl
Cytoband20p11.1
Allele length
AssemblyAllele length
hg38161794
hg19161794
hg18161794
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv585756
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)nssv938985
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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