A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14106366



Internal ID21284340
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 StatusS
Merged Variantsnsv3111925
Supporting Variants
Samplessample360
Known GenesTBR1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14106366
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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