A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17742874



Internal ID166540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:20136507..20325982hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38189476
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5417842
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17742874
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.994997


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