A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110305



Internal ID21293571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:671030..672982hg38UCSC Ensembl
Innerchr18:671030..672982hg19UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg381953
hg191953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14100959, nssv14099331, nssv14100158
Samplessample156, sample402, sample290
Known GenesENOSF1, TYMS
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110305
Frequency
Sample Size467
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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