A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5848418



Internal ID22623353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:28453171..28455006hg38UCSC Ensembl
chr8:28310688..28312523hg19UCSC Ensembl
Cytoband8p21.1
Allele length
AssemblyAllele length
hg381836
hg191836
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17508753
Samples
Known GenesFBXO16
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5848418
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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