A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5990680



Internal ID21900023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:9810747..9842241hg38UCSC Ensembl
chr2:9950876..9982370hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg3831495
hg1931495
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17519190
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5990680
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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