A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112774



Internal ID21296040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:296068..382543hg38UCSC Ensembl
Innerchr6:296068..382543hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3886476
hg1986476
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1005n145
Supporting Variantsnssv14083902, nssv14082883
Samplessample303, sample402
Known GenesDUSP22
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112774
Frequency
Sample Size467
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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