A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5919293



Internal ID22694515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:124037301..124050751hg38UCSC Ensembl
chr11:123908008..123921458hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg3813451
hg1913451
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17354042
Samples
Known GenesOR10G7
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5919293
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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