A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115239



Internal ID21298505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:24847782..24849585hg38UCSC Ensembl
Innerchr15:25092929..25094732hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg381804
hg191804
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv388n145
Supporting Variantsnssv14095954
Samplessample37
Known GenesSNRPN
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115239
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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