A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6089647



Internal ID21998880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:18271120..18271120hg38UCSC Ensembl
chrUn_gl000212:99872..99872hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17607987
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6089647
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