A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117290



Internal ID21300556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:28210282..28213639hg38UCSC Ensembl
Innerchr16:28221603..28224960hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg383358
hg193358
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14099135, nssv14096444
Samplessample149, sample289
Known GenesXPO6
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117290
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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