A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16991237



Internal ID61558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:166901072..166902146hg38UCSC Ensembl
chr6:167314560..167315634hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg381075
hg191075
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5469086
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16991237
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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