A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116774



Internal ID21300040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:341234..360249hg38UCSC Ensembl
Innerchr6:341234..360249hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3819016
hg1919016
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14089192
Samplessample279
Known GenesDUSP22
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116774
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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