A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17742883



Internal ID166549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:20204634..20315295hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38110662
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5424164
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17742883
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00375235


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