A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5517086



Internal ID293516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:33794413..33795047hg38UCSC Ensembl
chr20:32382219..32382853hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg38635
hg19635
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17732050
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5517086
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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