A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14094558



Internal ID21268858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:52886981..52895342hg38UCSC Ensembl
Innerchr13:53461116..53469477hg19UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg388362
hg198362
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115749
Supporting Variants
Samplessample130
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14094558
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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