A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6090587



Internal ID21999820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:33750919..33750919hg38UCSC Ensembl
chr11:33772465..33772465hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38302
hg19302
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17589887
Samples
Known GenesFBXO3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6090587
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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