A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17728730



Internal ID152396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:35724123..35724126hg38UCSC Ensembl
chr22:36120170..36120173hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38254
hg19254
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5418831
Supporting Variants
Samples
Known GenesAPOL5
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17728730
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001093


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