A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5989161



Internal ID21898504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:41288757..41586263hg38UCSC Ensembl
chr2:41515897..41813403hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg38297507
hg19297507
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17520748
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5989161
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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