A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5562674



Internal ID335620
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 StatusM
Merged Variants
Supporting Variantsnssv17015771
Samples
Known GenesUBR5
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5562674
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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