A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14092926



Internal ID21271361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:20317580..20321090hg38UCSC Ensembl
Innerchr12:20470514..20474024hg19UCSC Ensembl
Cytoband12p12.2
Allele length
AssemblyAllele length
hg383511
hg193511
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115273
Supporting Variants
Samplessample162
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14092926
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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