A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115749



Internal ID21299015
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 StatusM
Merged Variants
Supporting Variantsnssv14094558
Samplessample130
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115749
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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