A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14094046



Internal ID21273323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:102823035..102841070hg38UCSC Ensembl
Innerchr14:103289372..103307407hg19UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg3818036
hg1918036
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115346
Supporting Variants
Samplessample19
Known GenesTRAF3
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14094046
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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