A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5666067



Internal ID21614372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:138157333..138384716hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38227384
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17161691
SamplesHG02818
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5666067
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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