A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17010325



Internal ID74515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:23211646..23211788hg38UCSC Ensembl
chr8:23069159..23069301hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg38143
hg19143
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5488476
Supporting Variants
Samples
Known GenesTNFRSF10A
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17010325
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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