A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6104262



Internal ID22013495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:46283273..47379106hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg381095834
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17581055
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6104262
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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