A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521439



Internal ID15448732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:69122652..69136589hg38UCSC Ensembl
Innerchr3:69171803..69185740hg19UCSC Ensembl
Innerchr3:69254493..69268430hg18UCSC Ensembl
Innerchr3:69254493..69268430hg17UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3813938
hg1913938
hg1813938
hg1713938
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698049
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521439
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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