A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5920416



Internal ID22695639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:7491543..7491764hg38UCSC Ensembl
chr11:7512774..7512995hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38222
hg19222
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17358119
Samples
Known GenesOLFML1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5920416
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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