A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6098199



Internal ID22007432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:110452059..110452059hg38UCSC Ensembl
chr11:110322783..110322783hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38137
hg19137
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17612079
Samples
Known GenesFDX1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6098199
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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