A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6082836



Internal ID21992069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:122359772..122359772hg38UCSC Ensembl
chr9:125122051..125122051hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg38167
hg19167
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17596424
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6082836
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