A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5993077



Internal ID21902420
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:27632888..27632939hg38UCSC Ensembl
chr3:27674379..27674430hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17545910
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5993077
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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