A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5517951



Internal ID294353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:60756699..60756785hg38UCSC Ensembl
chr20:59331756..59331842hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3887
hg1987
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17733437
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5517951
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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