A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5988042



Internal ID21897385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:236770197..236778853hg38UCSC Ensembl
chr2:237678840..237687496hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg388657
hg198657
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17518326
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5988042
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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