A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6098567



Internal ID22007800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:33766091..33766091hg38UCSC Ensembl
chr11:33787637..33787637hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38240
hg19240
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17587548
Samples
Known GenesFBXO3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6098567
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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