A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6089085



Internal ID21998318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:51858068..51858068hg38UCSC Ensembl
chr16:51891979..51891979hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17636797
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6089085
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