A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565967



Internal ID16006690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:102777302..102778238hg38UCSC Ensembl
Innerchr14:103243639..103244575hg19UCSC Ensembl
Innerchr14:102313392..102314328hg18UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg38937
hg19937
hg18937
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3933n54
Supporting Variantsnssv834312, nssv834309, nssv834313, nssv834311, nssv834310, nssv834314
Samples
Known GenesTRAF3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565967
Frequency
Sample Size17421
Observed Gain3
Observed Loss3
Observed Complex0
Frequencyn/a


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