A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv668761



Internal ID15405413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:35781787..35897303hg38UCSC Ensembl
Innerchr3:35823279..35938795hg19UCSC Ensembl
Innerchr3:35798283..35913799hg18UCSC Ensembl
Innerchr3:35798283..35913799hg17UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg38115517
hg19115517
hg18115517
hg17115517
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516510
Supporting Variants
Samples
Known GenesARPP21
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv668761
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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