A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112169



Internal ID21295435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:76531070..76546294hg38UCSC Ensembl
Innerchr2:76758196..76773420hg19UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg3815225
hg1915225
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14105164
Samplessample263
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112169
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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