A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697114



Internal ID15087080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:31509375..31691041hg38UCSC Ensembl
Innerchr21:32881688..33063354hg19UCSC Ensembl
Innerchr21:31803559..31985225hg18UCSC Ensembl
Innerchr21:31803559..31985225hg17UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg38181667
hg19181667
hg18181667
hg17181667
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519899
Supporting Variants
Samples
Known GenesSCAF4, SOD1, TIAM1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697114
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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