A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696236



Internal ID15432888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:34567115..34569260hg38UCSC Ensembl
Innerchr21:35939413..35941558hg19UCSC Ensembl
Innerchr21:34861283..34863428hg18UCSC Ensembl
Innerchr21:34861283..34863428hg17UCSC Ensembl
Cytoband21q22.12
Allele length
AssemblyAllele length
hg382146
hg192146
hg182146
hg172146
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518782
Supporting Variants
Samples
Known GenesRCAN1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696236
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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