A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17015892



Internal ID78242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:106338340..106339213hg38UCSC Ensembl
chr8:107350568..107351441hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg38874
hg19874
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5489684
Supporting Variants
Samples
Known GenesOXR1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17015892
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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