A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv211n206



Internal ID22755515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:88276682..88282341hg38UCSC Ensembl
chr16:88310288..88315947hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg385660
hg195660
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6145503, nsv6145116
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)dgv211n206
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