A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527598



Internal ID15454891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:80536305..81201512hg38UCSC Ensembl
Innerchr3:80585455..81250663hg19UCSC Ensembl
Innerchr3:80668145..81333353hg18UCSC Ensembl
Innerchr3:80668145..81333353hg17UCSC Ensembl
Cytoband3p12.2
Allele length
AssemblyAllele length
hg38665208
hg19665209
hg18665209
hg17665209
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704060
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527598
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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