A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17731933



Internal ID155599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:32039960..32039960hg38UCSC Ensembl
chr20:30627763..30627763hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg38293
hg19293
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5433223
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17731933
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.01864


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