A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14094452



Internal ID21291776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:90886472..90887637hg38UCSC Ensembl
Innerchr13:91538726..91539891hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg381166
hg191166
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3113236
Supporting Variants
Samplessample79
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14094452
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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