A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6003413



Internal ID21912756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:28479558..28483430hg38UCSC Ensembl
chr8:28337075..28340947hg19UCSC Ensembl
Cytoband8p21.1
Allele length
AssemblyAllele length
hg383873
hg193873
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17572667
Samples
Known GenesFBXO16
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6003413
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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