A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565957



Internal ID16006680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:102777002..102778185hg38UCSC Ensembl
Innerchr14:103243339..103244522hg19UCSC Ensembl
Innerchr14:102313092..102314275hg18UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg381184
hg191184
hg181184
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3933n54
Supporting Variantsnssv834264, nssv834262, nssv834267, nssv834266, nssv834263, nssv834271, nssv834268, nssv834273, nssv834269, nssv834275, nssv834274, nssv834265, nssv834270, nssv834272
Samples
Known GenesTRAF3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565957
Frequency
Sample Size17421
Observed Gain12
Observed Loss2
Observed Complex0
Frequencyn/a


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