A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115705



Internal ID21298971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:46511725..46517129hg38UCSC Ensembl
Innerchr13:47085860..47091264hg19UCSC Ensembl
Cytoband13q14.13
Allele length
AssemblyAllele length
hg385405
hg195405
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv290n145
Supporting Variantsnssv14094607, nssv14092992, nssv14094526, nssv14094528
Samplessample152, sample417, sample112, sample113
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115705
Frequency
Sample Size467
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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