A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701232



Internal ID15437884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:72327657..72329582hg38UCSC Ensembl
Innerchr3:72376808..72378733hg19UCSC Ensembl
Innerchr3:72459498..72461423hg18UCSC Ensembl
Innerchr3:72459498..72461423hg17UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg381926
hg191926
hg181926
hg171926
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515782
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701232
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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