A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114952



Internal ID21298218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:58891133..58914327hg38UCSC Ensembl
Innerchr8:59803692..59826886hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg3823195
hg1923195
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14087023
Samplessample97
Known GenesTOX
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114952
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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