A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112921



Internal ID21296187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:83340478..83405588hg38UCSC Ensembl
Innerchr13:83914613..83979723hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3865111
hg1965111
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14092957
Samplessample396
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112921
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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