A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6099077



Internal ID22008310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:69363117..69363117hg38UCSC Ensembl
chr11:69177885..69177885hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17585493
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6099077
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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