A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5992399



Internal ID21901742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:182881390..182881442hg38UCSC Ensembl
chr3:182599178..182599230hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17540958
Samples
Known GenesATP11B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5992399
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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