A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5536891



Internal ID312298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:45284674..45290669hg38UCSC Ensembl
chr22:45680555..45686550hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg385996
hg195996
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17729477
Samples
Known GenesUPK3A
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5536891
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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