A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115381



Internal ID21298647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:18853258..18859688hg38UCSC Ensembl
Innerchr12:19006192..19012622hg19UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg386431
hg196431
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14093297
Samplessample425
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115381
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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