A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv563811



Internal ID16351220
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19925415..19990148hg38UCSC Ensembl
Innerchr14:20393574..20458307hg19UCSC Ensembl
Innerchr14:19463414..19528147hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3864734
hg1964734
hg1864734
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3531n54
Supporting Variantsnssv821710, nssv821709
Samples
Known GenesOR4K1, OR4K15
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv563811
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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