A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520776



Internal ID15448069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:8913275..8947125hg38UCSC Ensembl
Innerchr3:8954959..8988809hg19UCSC Ensembl
Innerchr3:8929959..8963809hg18UCSC Ensembl
Innerchr3:8929959..8963809hg17UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg3833851
hg1933851
hg1833851
hg1733851
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697603
Samples
Known GenesRAD18
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520776
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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