A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565960



Internal ID16006683
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:102777054..102778134hg38UCSC Ensembl
Innerchr14:103243391..103244471hg19UCSC Ensembl
Innerchr14:102313144..102314224hg18UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg381081
hg191081
hg181081
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3933n54
Supporting Variantsnssv834289, nssv834291, nssv834292, nssv834290
Samples
Known GenesTRAF3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565960
Frequency
Sample Size17421
Observed Gain3
Observed Loss1
Observed Complex0
Frequencyn/a


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