A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16984905



Internal ID57322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:50172094..50186079hg38UCSC Ensembl
chr6:50139807..50153792hg19UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg3813986
hg1913986
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5463343
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16984905
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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