A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv566141



Internal ID16006864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:104938047..105089059hg38UCSC Ensembl
Innerchr14:105404384..105555396hg19UCSC Ensembl
Innerchr14:104475429..104626441hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38151013
hg19151013
hg18151013
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv834715
Samples
Known GenesAHNAK2, C14orf79, CDCA4, GPR132
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv566141
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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