A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5546881



Internal ID320785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:27101988..27110224hg38UCSC Ensembl
chr22:27497950..27506186hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg388237
hg198237
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17728228
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5546881
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