A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16986257



Internal ID58263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:103964397..104007721hg38UCSC Ensembl
chr6:104412272..104455596hg19UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg3843325
hg1943325
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5463887
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16986257
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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