A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14096936



Internal ID21283738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:77025164..77027834hg38UCSC Ensembl
Innerchr13:77599299..77601969hg19UCSC Ensembl
Cytoband13q22.3
Allele length
AssemblyAllele length
hg382671
hg192671
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3116331
Supporting Variants
Samplessample349
Known GenesFBXL3
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14096936
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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