A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17094589



Internal ID21410422
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 StatusS
Merged Variantsnsv5669080
Supporting Variants
SamplesHG00513
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17094589
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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