A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110918



Internal ID21294184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:59394126..59400236hg38UCSC Ensembl
Innerchr14:59860844..59866954hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg386111
hg196111
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14094022, nssv14094058
Samplessample9, sample25
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110918
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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