A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16986801



Internal ID58640
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:113432996..113448554hg38UCSC Ensembl
chr6:113754198..113769756hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3815559
hg1915559
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5459993
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16986801
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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