A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17586649



Internal ID21778692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:3096909..3097168hg38UCSC Ensembl
chr11:3118139..3118398hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38260
hg19260
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6035967
Supporting Variants
Samples
Known GenesOSBPL5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17586649
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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