A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5993168



Internal ID21902511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:25484156..25484447hg38UCSC Ensembl
chr3:25525647..25525938hg19UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg38292
hg19292
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17538600
Samples
Known GenesRARB
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5993168
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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