A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694971



Internal ID15431623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:28140267..28376656hg38UCSC Ensembl
Innerchr21:29512586..29748977hg19UCSC Ensembl
Innerchr21:28434457..28670848hg18UCSC Ensembl
Innerchr21:28434457..28670848hg17UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg38236390
hg19236392
hg18236392
hg17236392
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522198
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694971
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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