A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16979080



Internal ID53433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:15998331..15998398hg38UCSC Ensembl
chr6:15998562..15998629hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5464122
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16979080
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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