A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111925



Internal ID21295191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:161422348..161430676hg38UCSC Ensembl
Innerchr2:162278859..162287187hg19UCSC Ensembl
Cytoband2q24.2
Allele length
AssemblyAllele length
hg388329
hg198329
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14106366
Samplessample360
Known GenesTBR1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111925
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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