A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694503



Internal ID15431155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:104517677..104529556hg38UCSC Ensembl
Innerchr14:104984014..104995893hg19UCSC Ensembl
Innerchr14:104055059..104066938hg18UCSC Ensembl
Innerchr14:104055059..104066938hg17UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3811880
hg1911880
hg1811880
hg1711880
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521738
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694503
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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