A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5485789



Internal ID263171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:89944793..89951257hg38UCSC Ensembl
chr8:90957021..90963485hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg386465
hg196465
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17013522
Samples
Known GenesNBN
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5485789
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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