A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6038305



Internal ID21947648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:3096899..3096959hg38UCSC Ensembl
chr11:3118129..3118189hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17588258
Samples
Known GenesOSBPL5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6038305
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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