A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705165



Internal ID15441817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:83069036..83078087hg38UCSC Ensembl
Innerchr14:83535380..83544431hg19UCSC Ensembl
Innerchr14:82605133..82614184hg18UCSC Ensembl
Innerchr14:82605133..82614184hg17UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg389052
hg199052
hg189052
hg179052
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528552
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705165
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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