A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5665579



Internal ID21613884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:90117198..90328344hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38211147
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17092767
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5665579
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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