A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698473



Internal ID15435125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:35340208..35369183hg38UCSC Ensembl
Innerchr14:35809414..35838389hg19UCSC Ensembl
Innerchr14:34879165..34908140hg18UCSC Ensembl
Innerchr14:34879165..34908140hg17UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg3828976
hg1928976
hg1828976
hg1728976
Variant TypeCNV gain
Copy Number
Allele State
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)nssv698473
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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