A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv679493



Internal ID15416145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:35333277..35352486hg38UCSC Ensembl
Innerchr14:35802483..35821692hg19UCSC Ensembl
Innerchr14:34872234..34891443hg18UCSC Ensembl
Innerchr14:34872234..34891443hg17UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg3819210
hg1919210
hg1819210
hg1719210
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518090
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv679493
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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