A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv566237



Internal ID16353646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:105474226..105485274hg38UCSC Ensembl
Innerchr14:105940563..105951611hg19UCSC Ensembl
Innerchr14:105011608..105022656hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3811049
hg1911049
hg1811049
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3996n54
Supporting Variantsnssv834878
Samples
Known GenesCRIP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv566237
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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