A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17012102



Internal ID75738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:73821596..73822030hg38UCSC Ensembl
chr8:74733831..74734265hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg38435
hg19435
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5554322
Supporting Variants
Samples
Known GenesUBE2W
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17012102
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.018108


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