A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565969



Internal ID16006692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:102777444..102778238hg38UCSC Ensembl
Innerchr14:103243781..103244575hg19UCSC Ensembl
Innerchr14:102313534..102314328hg18UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg38795
hg19795
hg18795
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv834316
Samples
Known GenesTRAF3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565969
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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