A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17726997



Internal ID150663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:41474010..41475052hg38UCSC Ensembl
chr21:42845937..42846979hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg381043
hg191043
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5534360
Supporting Variants
Samples
Known GenesTMPRSS2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17726997
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000624


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