A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115156



Internal ID21298422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:138802124..138828927hg38UCSC Ensembl
Innerchr2:139559694..139586497hg19UCSC Ensembl
Cytoband2q22.1
Allele length
AssemblyAllele length
hg3826804
hg1926804
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14106778
Samplessample368
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115156
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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