A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6079587



Internal ID21988820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:166640304..166640304hg38UCSC Ensembl
chr6:167053792..167053792hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg381367
hg191367
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17561129
Samples
Known GenesRPS6KA2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6079587
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