A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5562257



Internal ID335215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:36225334..36268354hg38UCSC Ensembl
chr22:36621380..36664400hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3843021
hg1943021
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17728761
Samples
Known GenesAPOL1, APOL2
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5562257
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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