A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520836



Internal ID15448129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:27454979..27558719hg38UCSC Ensembl
Innerchr14:27924185..28027925hg19UCSC Ensembl
Innerchr14:26994025..27097765hg18UCSC Ensembl
Innerchr14:26994025..27097765hg17UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38103741
hg19103741
hg18103741
hg17103741
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704945, nssv703864, nssv705312, nssv704538, nssv693162, nssv676279
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520836
Frequency
Sample Size2026
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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