A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14092085



Internal ID21274497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:15654538..15657788hg38UCSC Ensembl
Innerchr4:15656161..15659411hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg383251
hg193251
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3116176
Supporting Variants
Samplessample208
Known GenesFBXL5
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14092085
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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