A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695161



Internal ID15431813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:49346080..49362991hg38UCSC Ensembl
Innerchr14:49812798..49829709hg19UCSC Ensembl
Innerchr14:48882548..48899459hg18UCSC Ensembl
Innerchr14:48882548..48899459hg17UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg3816912
hg1916912
hg1816912
hg1716912
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522381
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695161
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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