A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5544766



Internal ID318878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:36137564..36187564hg38UCSC Ensembl
chr22:36533612..36583612hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3850001
hg1950001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17728754
Samples
Known GenesAPOL3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5544766
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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