A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5993463



Internal ID21902806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:43479058..43479144hg38UCSC Ensembl
chr3:43520550..43520636hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg3887
hg1987
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17548717
Samples
Known GenesANO10
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5993463
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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