A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5666496



Internal ID21614801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:46398630..47461135hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg381062506
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17070061
Samples
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5666496
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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