A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5993123



Internal ID21902466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:36634387..36634613hg38UCSC Ensembl
chr3:36675879..36676105hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg38227
hg19227
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17547549
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5993123
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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