A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4389658



Internal ID21380793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:5476752..5477271hg38UCSC Ensembl
chr11:5497982..5498501hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38520
hg19520
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15705022
Samples
Known GenesOR51B5
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4389658
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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