A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv656933



Internal ID15046899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:63313998..63391090hg38UCSC Ensembl
Innerchr14:63780711..63857808hg19UCSC Ensembl
Innerchr14:62850464..62927561hg18UCSC Ensembl
Innerchr14:62850464..62927561hg17UCSC Ensembl
Cytoband14q23.2
Allele length
AssemblyAllele length
hg3877093
hg1977098
hg1877098
hg1777098
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519574
Supporting Variants
Samples
Known GenesGPHB5, PPP2R5E
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv656933
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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