A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6092284



Internal ID22001517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:10884128..10884128hg38UCSC Ensembl
chr16:10977985..10977985hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg38989
hg19989
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17617114
Samples
Known GenesCIITA
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6092284
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