A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111531



Internal ID21294797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:5869301..5889793hg38UCSC Ensembl
Innerchr2:6009433..6029925hg19UCSC Ensembl
Cytoband2p25.2
Allele length
AssemblyAllele length
hg3820493
hg1920493
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14104067
Samplessample7
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111531
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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