A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17050640



Internal ID101641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:107041385..107227716hg38UCSC Ensembl
chr11:106912111..107098442hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38186332
hg19186332
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5512116
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17050640
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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