A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116223



Internal ID21299489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:183593723..184303116hg38UCSC Ensembl
Innerchr2:184458451..185167843hg19UCSC Ensembl
Cytoband2q32.1
Allele length
AssemblyAllele length
hg38709394
hg19709393
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14106231
Samplessample331
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116223
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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