A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111125



Internal ID21294391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:17500574..17554457hg38UCSC Ensembl
Innerchr10:17542573..17596456hg19UCSC Ensembl
Cytoband10p12.33
Allele length
AssemblyAllele length
hg3853884
hg1953884
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14088904
Samplessample3
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111125
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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