A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115616



Internal ID21298882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:51748653..51754471hg38UCSC Ensembl
Innerchr15:52040850..52046668hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg385819
hg195819
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv404n145
Supporting Variantsnssv14095287
Samplessample10
Known GenesLYSMD2, TMOD2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115616
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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