A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6093758



Internal ID22002991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:128868087..128868087hg38UCSC Ensembl
chr11:128737982..128737982hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg382251
hg192251
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17600575
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6093758
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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