A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516141



Internal ID15096748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:76203693..76205608hg38UCSC Ensembl
Innerchr14:76670036..76671951hg19UCSC Ensembl
Innerchr14:75739789..75741704hg18UCSC Ensembl
Innerchr14:75739789..75741704hg17UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg381916
hg191916
hg181916
hg171916
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv666449, nssv683103
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516141
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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