A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117326



Internal ID21300592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:131947789..131953571hg38UCSC Ensembl
Innerchr6:132268929..132274711hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg385783
hg195783
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1071n145
Supporting Variantsnssv14083162, nssv14083913, nssv14082874, nssv14083878
Samplessample404, sample300, sample378, sample397
Known GenesCTGF
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117326
Frequency
Sample Size467
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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