A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv539n206



Internal ID22755843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:28533625..28762059hg38UCSC Ensembl
chr9:28533623..28762057hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38228435
hg19228435
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5480528, nsv5480938
Samples
Known GenesLINGO2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)dgv539n206
Frequency
Sample Size3202
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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