A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6109860



Internal ID22019093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:44229616..44229616hg38UCSC Ensembl
chr21:45649499..45649499hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38115
hg19115
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17643341
Samples
Known GenesICOSLG
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6109860
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