A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv503n206



Internal ID22755807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:6020470..6377261hg38UCSC Ensembl
chr8:5877992..6234782hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38356792
hg19356791
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5474533, nsv5489122
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)dgv503n206
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