A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17361351



Internal ID22587020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:89174074..89539687hg38UCSC Ensembl
chr11:88907242..89272855hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg38365614
hg19365614
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5910300
Supporting Variants
Samples
Known GenesNOX4, TYR
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17361351
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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