A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17526537



Internal ID21850895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:240354486..240354894hg38UCSC Ensembl
chr2:241293903..241294311hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg38409
hg19409
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5988756
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17526537
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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