A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16991017



Internal ID61424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:168158789..168251949hg38UCSC Ensembl
chr6:168559469..168652629hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3893161
hg1993161
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5466257
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16991017
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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