A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17034366



Internal ID90606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:56941211..56941372hg38UCSC Ensembl
chr10:58700971..58701132hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38162
hg19162
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5486933
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17034366
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000781


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