A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17419395



Internal ID22477265
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 StatusS
Merged Variantsnsv5890465
Supporting Variants
Samples
Known GenesFBXL7
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17419395
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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