A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3589634



Internal ID18887915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:35762271..35907323hg38UCSC Ensembl
Innerchr3:35803763..35948815hg19UCSC Ensembl
Innerchr3:35778767..35923819hg18UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg38145053
hg19145053
hg18145053
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv997763
Supporting Variants
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)nssv3589634
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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