A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115451



Internal ID21298717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:106671751..106680781hg38UCSC Ensembl
Innerchr6:107119626..107128656hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg389031
hg199031
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1061n145
Supporting Variantsnssv14082865
Samplessample299
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115451
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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