A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5665280



Internal ID21613585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:146327105..149352353hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg383025249
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17061122
Samples
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5665280
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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