A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17059152



Internal ID107303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:88004896..88070896hg38UCSC Ensembl
chr11:87738379..87804064hg19UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg3866001
hg1965686
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5506691
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17059152
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000313


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