A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117376



Internal ID21300642
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 StatusM
Merged Variantsdgv1005n145
Supporting Variantsnssv14089171, nssv14086367
Samplessample130, sample275
Known GenesDUSP22
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117376
Frequency
Sample Size467
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer