A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565966



Internal ID16006689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:102777302..102778185hg38UCSC Ensembl
Innerchr14:103243639..103244522hg19UCSC Ensembl
Innerchr14:102313392..102314275hg18UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg38884
hg19884
hg18884
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3933n54
Supporting Variantsnssv834306, nssv834304, nssv834305, nssv834307, nssv834308
Samples
Known GenesTRAF3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565966
Frequency
Sample Size17421
Observed Gain2
Observed Loss3
Observed Complex0
Frequencyn/a


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