A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6105776



Internal ID22015009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:21086710..21089183hg38UCSC Ensembl
chr20:21067351..21069824hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg382474
hg192474
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17622237
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6105776
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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