A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5910300



Internal ID22685511
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 StatusM
Merged Variants
Supporting Variantsnssv17361351
Samples
Known GenesNOX4, TYR
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5910300
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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