A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1086n145



Internal ID22814102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:169063796..169065866hg38UCSC Ensembl
chr6:169463891..169465961hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg382071
hg192071
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3112710, nsv3112480
Samplessample270, sample56
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv1086n145
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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