A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5993366



Internal ID21902709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:40077465..40077518hg38UCSC Ensembl
chr3:40118956..40119009hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17542142
Samples
Known GenesMYRIP
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5993366
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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