A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700184



Internal ID15436836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:35358173..35369638hg38UCSC Ensembl
Innerchr21:36730471..36741936hg19UCSC Ensembl
Innerchr21:35652341..35663806hg18UCSC Ensembl
Innerchr21:35652341..35663806hg17UCSC Ensembl
Cytoband21q22.12
Allele length
AssemblyAllele length
hg3811466
hg1911466
hg1811466
hg1711466
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524285
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700184
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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