A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16986354



Internal ID58333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:109020949..109021098hg38UCSC Ensembl
chr6:109342152..109342301hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38150
hg19150
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5472366
Supporting Variants
Samples
Known GenesSESN1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16986354
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer