A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv60n206



Internal ID22755364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:78090368..78098368hg38UCSC Ensembl
chr10:79850125..79858125hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg388001
hg198001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5482621, nsv5490333
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)dgv60n206
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