A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5669080



Internal ID21617385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:18408216..18477230hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3869015
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17094589
SamplesHG00513
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5669080
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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