A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17519438



Internal ID21843797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:19376560..19385705hg38UCSC Ensembl
chr2:19576321..19585466hg19UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg389146
hg199146
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5987223
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17519438
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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