A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703983



Internal ID15440635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:46057951..46071100hg38UCSC Ensembl
Innerchr21:47477865..47491014hg19UCSC Ensembl
Innerchr21:46302293..46315442hg18UCSC Ensembl
Innerchr21:46302293..46315442hg17UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3813150
hg1913150
hg1813150
hg1713150
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519834
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703983
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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