A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5481106



Internal ID258601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:106572257..106572383hg38UCSC Ensembl
chr8:107584485..107584611hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg38127
hg19127
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17015914
Samples
Known GenesOXR1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5481106
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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