A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1868n71



Internal ID6319488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:29189774..29257152hg19UCSC Ensembl
chr14:28259525..28326903hg18UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnsv901576, nsv901577, nsv901575
SamplesIS35789, MS20710, IS35572
Known GenesC14orf23, FOXG1
Method
Analysis
Platform
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)dgv1868n71
Frequency
Sample Size6533
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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