A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5992827



Internal ID21902170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:20106977..20107031hg38UCSC Ensembl
chr3:20148469..20148523hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17541515
Samples
Known GenesKAT2B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5992827
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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