A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17406363



Internal ID22464233
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 StatusS
Merged Variantsnsv5956933
Supporting Variants
Samples
Known GenesAPOL4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17406363
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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