A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113602



Internal ID21296868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:11015721..11020735hg38UCSC Ensembl
Innerchr10:11057684..11062698hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg385015
hg195015
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv140n145
Supporting Variantsnssv14088766
Samplessample308
Known GenesCELF2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113602
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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