A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16986711



Internal ID58581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:108284242..108286839hg38UCSC Ensembl
chr6:108605446..108608043hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg382598
hg192598
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5466599
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16986711
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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