A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565963



Internal ID16006686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:102777105..102778134hg38UCSC Ensembl
Innerchr14:103243442..103244471hg19UCSC Ensembl
Innerchr14:102313195..102314224hg18UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg381030
hg191030
hg181030
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3934n54
Supporting Variantsnssv834296
Samples
Known GenesTRAF3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565963
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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