A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17015895



Internal ID78243
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 StatusS
Merged Variantsnsv5560592
Supporting Variants
Samples
Known GenesOXR1
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17015895
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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