A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516510



Internal ID15443803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:35759275..35897303hg38UCSC Ensembl
Innerchr3:35800767..35938795hg19UCSC Ensembl
Innerchr3:35775771..35913799hg18UCSC Ensembl
Innerchr3:35775771..35913799hg17UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg38138029
hg19138029
hg18138029
hg17138029
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv688814, nssv668761, nssv655068
Samples
Known GenesARPP21
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516510
Frequency
Sample Size2026
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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