A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17518326



Internal ID21842685
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 StatusS
Merged Variantsnsv5988042
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17518326
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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