A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv563612



Internal ID16351021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:18574998..19061863hg38UCSC Ensembl
Innerchr14:19351475..19649523hg19UCSC Ensembl
Innerchr14:18421475..18719523hg18UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg38486866
hg19298049
hg18298049
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3496n54
Supporting Variantsnssv821327
Samples
Known GenesLOC642426, OR11H12, POTEG
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv563612
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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