A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4617n223



Internal ID22807585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:12027601..12069300hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3841700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6542383, nsv6554757, nsv6536969
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv4617n223
Frequency
Sample Size19652
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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