A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5580989



Internal ID21529485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:28453201..28454995hg38UCSC Ensembl
chr8:28310718..28312512hg19UCSC Ensembl
Cytoband8p21.1
Allele length
AssemblyAllele length
hg381795
hg191795
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17144585
SamplesHG03065
Known GenesFBXO16
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5580989
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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