A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14105615



Internal ID21289002
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 StatusS
Merged Variantsnsv3115851
Supporting Variants
Samplessample424
Known GenesARHGEF3
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14105615
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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