A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117047



Internal ID21300313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:11016257..11020735hg38UCSC Ensembl
Innerchr10:11058220..11062698hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg384479
hg194479
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv140n145
Supporting Variantsnssv14088661
Samplessample245
Known GenesCELF2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117047
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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