A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110861



Internal ID21294127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:71688183..71698228hg38UCSC Ensembl
Innerchr15:71980522..71990567hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3810046
hg1910046
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv410n145
Supporting Variantsnssv14097189
Samplessample357
Known GenesTHSD4
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110861
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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