A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5916103



Internal ID22691322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:3113209..3115090hg38UCSC Ensembl
chr11:3134439..3136320hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg381882
hg191882
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17354841
Samples
Known GenesOSBPL5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5916103
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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