A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5991861



Internal ID21901204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:160426572..160426679hg38UCSC Ensembl
chr3:160144360..160144467hg19UCSC Ensembl
Cytoband3q25.33
Allele length
AssemblyAllele length
hg38108
hg19108
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17544064
Samples
Known GenesSMC4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5991861
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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