A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14108646



Internal ID21285323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:72101443..72114584hg38UCSC Ensembl
Innerchr3:72150594..72163735hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg3813142
hg1913142
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115844
Supporting Variants
Samplessample372
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14108646
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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