A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5987425



Internal ID21896768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:209033462..209365510hg38UCSC Ensembl
chr2:209898186..210230234hg19UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg38332049
hg19332049
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17535481
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5987425
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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