A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5890465



Internal ID22665493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:15860297..15862543hg38UCSC Ensembl
chr5:15860406..15862652hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg382247
hg192247
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17419395
Samples
Known GenesFBXL7
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5890465
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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