A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17586795



Internal ID21778838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:3112004..3112004hg38UCSC Ensembl
chr11:3133234..3133234hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38114
hg19114
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6094590
Supporting Variants
Samples
Known GenesOSBPL5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17586795
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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