A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1061n145



Internal ID22814077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:106671751..106680781hg38UCSC Ensembl
chr6:107119626..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 Variants
Supporting Variantsnsv3114472, nsv3115451
Samplessample299, sample61
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv1061n145
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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