A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565952



Internal ID16006675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:102776388..102778185hg38UCSC Ensembl
Innerchr14:103242725..103244522hg19UCSC Ensembl
Innerchr14:102312478..102314275hg18UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg381798
hg191798
hg181798
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3932n54
Supporting Variantsnssv834248, nssv834247, nssv834249
Samples
Known GenesTRAF3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565952
Frequency
Sample Size17421
Observed Gain1
Observed Loss2
Observed Complex0
Frequencyn/a


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