A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv518n206



Internal ID22755822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:609437..722197hg38UCSC Ensembl
chr9:609437..722197hg19UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg38112761
hg19112761
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5491607, nsv5478513
Samples
Known GenesKANK1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)dgv518n206
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