A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5478180



Internal ID255745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:58432858..58433190hg38UCSC Ensembl
chr8:59345417..59345749hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg38333
hg19333
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17012420
Samples
Known GenesUBXN2B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5478180
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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