A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4766958



Internal ID20542818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:24266034..24266690hg38UCSC Ensembl
chr11:24287580..24288236hg19UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg38657
hg19657
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16267087
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4766958
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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