A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6083819



Internal ID21993052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:46466222..46466222hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3867
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17595966
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6083819
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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