A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17731596



Internal ID155262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:22973097..22976451hg38UCSC Ensembl
chr20:22953734..22957088hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg383355
hg193355
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6146226
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17731596
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001562


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