A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111021



Internal ID21294287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:66799465..66807362hg38UCSC Ensembl
Innerchr3:66849889..66857786hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg387898
hg197898
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14106699
Samplessample191
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111021
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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