A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5988705



Internal ID21898048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:25346121..25354467hg38UCSC Ensembl
chr2:25568990..25577336hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg388347
hg198347
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17520491
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5988705
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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