A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17015771



Internal ID78159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:102352134..102512969hg38UCSC Ensembl
chr8:103364362..103525197hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg38160836
hg19160836
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5562674
Supporting Variants
Samples
Known GenesUBR5
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17015771
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000312


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