A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526865



Internal ID15454158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:34656805..34657635hg38UCSC Ensembl
Innerchr3:34698297..34699127hg19UCSC Ensembl
Innerchr3:34673301..34674131hg18UCSC Ensembl
Innerchr3:34673301..34674131hg17UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg38831
hg19831
hg18831
hg17831
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703223
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526865
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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