A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5560592



Internal ID333597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:106364638..106441726hg38UCSC Ensembl
chr8:107376866..107453954hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg3877089
hg1977089
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17015895
Samples
Known GenesOXR1
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5560592
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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