A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16983559



Internal ID56418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:33814009..33814079hg38UCSC Ensembl
chr6:33781786..33781856hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5472520
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16983559
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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