A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5486426



Internal ID263792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:94422361..94423122hg38UCSC Ensembl
chr8:95434589..95435350hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg38762
hg19762
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17014560
Samples
Known GenesRAD54B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5486426
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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