A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14108414



Internal ID21269642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:135928674..135932607hg38UCSC Ensembl
Innerchr5:135264363..135268296hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg383934
hg193934
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3110968
Supporting Variants
Samplessample141
Known GenesFBXL21
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14108414
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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