A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515782



Internal ID15442839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:72327657..72329799hg38UCSC Ensembl
Innerchr3:72376808..72378950hg19UCSC Ensembl
Innerchr3:72459498..72461640hg18UCSC Ensembl
Innerchr3:72459498..72461640hg17UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg382143
hg192143
hg182143
hg172143
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv664760, nssv670858, nssv701232
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515782
Frequency
Sample Size2026
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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