A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6112400



Internal ID22021633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:80141791..80176111hg38UCSC Ensembl
chr16:80175688..80210008hg19UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg3834321
hg1934321
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17629257
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6112400
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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