A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5551080



Internal ID324566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:48357000..48362000hg38UCSC Ensembl
chr22:48752812..48757812hg19UCSC Ensembl
Cytoband22q13.32
Allele length
AssemblyAllele length
hg385001
hg195001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17729713
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5551080
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