A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv660406



Internal ID15397058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:43358503..43778538hg38UCSC Ensembl
Innerchr14:43827706..44247741hg19UCSC Ensembl
Innerchr14:42897456..43317491hg18UCSC Ensembl
Innerchr14:42897456..43317491hg17UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg38420036
hg19420036
hg18420036
hg17420036
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515592
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv660406
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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