A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14105365



Internal ID21267078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:163391079..163419517hg38UCSC Ensembl
Innerchr3:163108867..163137305hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3828439
hg1928439
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3113422
Supporting Variants
Samplessample108
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14105365
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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