A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5956933



Internal ID22732086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:36195340..36195390hg38UCSC Ensembl
chr22:36591386..36591436hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17406363
Samples
Known GenesAPOL4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5956933
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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