A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14086367



Internal ID21268859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:296068..380796hg38UCSC Ensembl
Innerchr6:296068..380796hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3884729
hg1984729
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3117376
Supporting Variants
Samplessample130
Known GenesDUSP22
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14086367
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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