A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115851



Internal ID21299117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:56812868..56842447hg38UCSC Ensembl
Innerchr3:56846896..56876475hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg3829580
hg1929580
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14105615
Samplessample424
Known GenesARHGEF3
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115851
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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