A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv496n206



Internal ID22755800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:60000..126000hg38UCSC Ensembl
chr8:10001..76000hg19UCSC Ensembl
Cytoband8p23.3
Allele length
AssemblyAllele length
hg3866001
hg1966000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6141816, nsv6142355
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)dgv496n206
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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