A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16991252



Internal ID61569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:167114106..167117008hg38UCSC Ensembl
chr6:167527594..167530496hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg382903
hg192903
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5471514
Supporting Variants
Samples
Known GenesCCR6
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16991252
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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