A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117093



Internal ID21300359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:87284572..87293655hg38UCSC Ensembl
Innerchr12:87678349..87687432hg19UCSC Ensembl
Cytoband12q21.32
Allele length
AssemblyAllele length
hg389084
hg199084
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14091402
Samplessample25
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117093
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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