A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113621



Internal ID21296887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:68054738..68081897hg38UCSC Ensembl
Innerchr13:68628870..68656029hg19UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg3827160
hg1927160
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14095930, nssv14094523
Samplessample111, sample339
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113621
Frequency
Sample Size467
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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