A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv546n206



Internal ID22755850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:78547206..78555380hg38UCSC Ensembl
chr9:81162122..81170296hg19UCSC Ensembl
Cytoband9q21.31
Allele length
AssemblyAllele length
hg388175
hg198175
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5492983, nsv5476468
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)dgv546n206
Frequency
Sample Size3202
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer