A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519032



Internal ID15446325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:31950982..31951116hg38UCSC Ensembl
Innerchr14:32420188..32420322hg19UCSC Ensembl
Innerchr14:31489939..31490073hg18UCSC Ensembl
Innerchr14:31489939..31490073hg17UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38135
hg19135
hg18135
hg17135
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696501
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519032
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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