A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1225n145



Internal ID22814241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:23289386..23297798hg38UCSC Ensembl
chr9:23289384..23297796hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg388413
hg198413
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3114382, nsv3110309, nsv3115301, nsv3115355, nsv3111721, nsv3117299
Samplessample90, sample222, sample78, sample312, sample41, sample71, sample5, sample157, sample424, sample304, sample1, sample259, sample251
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv1225n145
Frequency
Sample Size467
Observed Gain0
Observed Loss13
Observed Complex0
Frequencyn/a


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