A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5563388



Internal ID336322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:30755023..30759905hg38UCSC Ensembl
chr8:30612540..30617422hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg384883
hg194883
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17011232
Samples
Known GenesUBXN8
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5563388
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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