A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17014265



Internal ID77178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:98856017..98858720hg38UCSC Ensembl
chr8:99868245..99870948hg19UCSC Ensembl
Cytoband8q22.2
Allele length
AssemblyAllele length
hg382704
hg192704
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5486589
Supporting Variants
Samples
Known GenesSTK3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17014265
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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