A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117854



Internal ID21301120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:129960567..129976883hg38UCSC Ensembl
Innerchr10:131758831..131775147hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3816317
hg1916317
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14088710
Samplessample273
Known GenesEBF3
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117854
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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