A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14107858



Internal ID21279888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:41754889..41916325hg38UCSC Ensembl
Innerchr3:41796381..41957817hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg38161437
hg19161437
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115447
Supporting Variants
Samplessample290
Known GenesULK4
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14107858
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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