A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17052411



Internal ID102786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:112599248..112599342hg38UCSC Ensembl
chr11:112469971..112470065hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg3895
hg1995
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5504713
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17052411
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.002029


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