A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697278



Internal ID15087244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:106492649..106621300hg38UCSC Ensembl
Innerchr14:106948660..107077314hg19UCSC Ensembl
Innerchr14:106019705..106148359hg18UCSC Ensembl
Innerchr14:106019705..106148359hg17UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38128652
hg19128655
hg18128655
hg17128655
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517055
Supporting Variants
Samples
Known GenesLINC00221
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697278
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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