A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7405n223



Internal ID22810373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:84612501..84618400hg38UCSC Ensembl
chr8:85524736..85530635hg19UCSC Ensembl
Cytoband8q21.2
Allele length
AssemblyAllele length
hg385900
hg195900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6434678, nsv6416236
Samples
Known GenesRALYL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv7405n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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