A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14092930



Internal ID21271357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:73291061..73393947hg38UCSC Ensembl
Innerchr12:73684841..73787727hg19UCSC Ensembl
Cytoband12q21.1
Allele length
AssemblyAllele length
hg38102887
hg19102887
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3117838
Supporting Variants
Samplessample162
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14092930
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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