A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17534858



Internal ID21859213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:189748790..189756997hg38UCSC Ensembl
chr2:190613516..190621723hg19UCSC Ensembl
Cytoband2q32.2
Allele length
AssemblyAllele length
hg388208
hg198208
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5987203
Supporting Variants
Samples
Known GenesOSGEPL1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17534858
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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