A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5988976



Internal ID21898319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:32068260..32072334hg38UCSC Ensembl
chr2:32293329..32297403hg19UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg384075
hg194075
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17528972
Samples
Known GenesSPAST
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5988976
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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