A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv563611



Internal ID16351020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:18574998..19014445hg38UCSC Ensembl
Innerchr14:19351475..19602149hg19UCSC Ensembl
Innerchr14:18421475..18672149hg18UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg38439448
hg19250675
hg18250675
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3496n54
Supporting Variantsnssv821326
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)nsv563611
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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