A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv548n206



Internal ID22755852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:128447990..128455326hg38UCSC Ensembl
chr9:131210269..131217605hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg387337
hg197337
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5481886, nsv6141548
Samples
Known GenesODF2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)dgv548n206
Frequency
Sample Size3202
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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