A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110640



Internal ID21293906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:102821242..102857099hg38UCSC Ensembl
Innerchr14:103287579..103323436hg19UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg3835858
hg1935858
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14095424
Samplessample163
Known GenesTRAF3
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110640
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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