A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6088566



Internal ID21997799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:110364049..110364049hg38UCSC Ensembl
chr11:110234774..110234774hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17604348
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6088566
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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