A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116513



Internal ID21299779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:48302738..48309942hg38UCSC Ensembl
Innerchr10:49510781..49517985hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg387205
hg197205
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv157n145
Supporting Variantsnssv14089931
Samplessample412
Known GenesMAPK8
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116513
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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