A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520387



Internal ID15447680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:24484796..24498614hg38UCSC Ensembl
Innerchr14:24954002..24967820hg19UCSC Ensembl
Innerchr14:24023842..24037660hg18UCSC Ensembl
Innerchr14:24023842..24037660hg17UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3813819
hg1913819
hg1813819
hg1713819
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv692745, nssv691222, nssv663539
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520387
Frequency
Sample Size2026
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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