A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565965



Internal ID16006688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:102777105..102778238hg38UCSC Ensembl
Innerchr14:103243442..103244575hg19UCSC Ensembl
Innerchr14:102313195..102314328hg18UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg381134
hg191134
hg181134
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3933n54
Supporting Variantsnssv834303, nssv834302
Samples
Known GenesTRAF3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565965
Frequency
Sample Size17421
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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