A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17538827



Internal ID21863182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:15586389..15586389hg38UCSC Ensembl
chr5:15586498..15586498hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6074162
Supporting Variants
Samples
Known GenesFBXL7
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17538827
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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