A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4372n223



Internal ID22807340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:11508401..11516600hg38UCSC Ensembl
chr20:11489049..11497248hg19UCSC Ensembl
Cytoband20p12.2
Allele length
AssemblyAllele length
hg388200
hg198200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6528721, nsv6527319
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv4372n223
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