A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112399



Internal ID21295665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:171149871..171152595hg38UCSC Ensembl
Innerchr1:171119010..171121734hg19UCSC Ensembl
Cytoband1q24.3
Allele length
AssemblyAllele length
hg382725
hg192725
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv85n145
Supporting Variantsnssv14089649
Samplessample241
Known GenesFMO6P
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112399
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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