A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv42n199



Internal ID22802928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:46382443..46396548hg38UCSC Ensembl
chr16:46416355..46430460hg19UCSC Ensembl
Cytoband16q11.2
Allele length
AssemblyAllele length
hg3814106
hg1914106
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv4762591, nsv4767797
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)dgv42n199
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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