A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7788n223



Internal ID22810756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:65059376..65068621hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg389246
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6448211, nsv6455072
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv7788n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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