A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1220n145



Internal ID22814236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:13570652..13576094hg38UCSC Ensembl
chr9:13570651..13576093hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg385443
hg195443
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3112532, nsv3112410, nsv3115543, nsv3117334
Samplessample322, sample365, sample167, sample170, sample420, sample180, sample9, sample156, sample142, sample87, sample125, sample314, sample165, sample202, sample312, sample400, sample143, sample58, sample414, sample291, sample181, sample186, sample59, sample320, sample390, sample169, sample19, sample44, sample5, sample81, sample424, sample118, sample233, sample243, sample18, sample318, sample89, sample250, sample99, sample46, sample162, sample246, sample268
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv1220n145
Frequency
Sample Size467
Observed Gain0
Observed Loss43
Observed Complex0
Frequencyn/a


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