A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18214496



Internal ID20781536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:135933751..135934107hg38UCSC Ensembl
chr5:135269440..135269796hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg38357
hg19357
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6413668
Supporting Variants
Samples
Known GenesFBXL21
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18214496
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.05626


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