A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110536



Internal ID21293802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:46323682..46370377hg38UCSC Ensembl
Innerchr13:46897817..46944512hg19UCSC Ensembl
Cytoband13q14.13
Allele length
AssemblyAllele length
hg3846696
hg1946696
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14094457
Samplessample81
Known GenesKIAA0226L
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110536
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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