A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17015094



Internal ID77721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:94949250..95000892hg38UCSC Ensembl
chr8:95961478..96013120hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg3851643
hg1951643
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5474867
Supporting Variants
Samples
Known GenesTP53INP1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17015094
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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