A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5667450



Internal ID21615755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:21558613..21610277hg38UCSC Ensembl
chr21:22930934..22982598hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg3851665
hg1951665
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17118773
Samples
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5667450
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