A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010151



Internal ID19099370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:35763779..35888171hg38UCSC Ensembl
Innerchr3:35805271..35929663hg19UCSC Ensembl
Innerchr3:35780275..35904667hg18UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg38124393
hg19124393
hg18124393
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4717n100
Supporting Variantsnssv3589638
Samples
Known GenesARPP21
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1010151
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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