A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110329



Internal ID21293595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:269534..360515hg38UCSC Ensembl
Innerchr6:269534..360515hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3890982
hg1990982
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1005n145
Supporting Variantsnssv14082877
Samplessample302
Known GenesDUSP22
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110329
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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