A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117052



Internal ID21300318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:109345787..109349327hg38UCSC Ensembl
Innerchr3:109064634..109068174hg19UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg383541
hg193541
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14103450
Samplessample15
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117052
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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