A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114837



Internal ID21298103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:58636713..58640128hg38UCSC Ensembl
Innerchr14:59103431..59106846hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg383416
hg193416
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv346n145
Supporting Variantsnssv14095574
Samplessample224
Known GenesDACT1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114837
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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