A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5991683



Internal ID21901026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:153881419..153896204hg38UCSC Ensembl
chr3:153599208..153613993hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg3814786
hg1914786
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17544096
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5991683
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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