A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5474867



Internal ID252517
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 StatusM
Merged Variants
Supporting Variantsnssv17015094
Samples
Known GenesTP53INP1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5474867
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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