A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17061122



Internal ID21512686
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 StatusS
Merged Variantsnsv5665280
Supporting Variants
Samples
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17061122
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer