A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5416n71



Internal ID6323036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:1707518..1901909hg19UCSC Ensembl
chr4:1677316..1871707hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnsv878396, nsv878398, nsv878395
SamplesIS33684, MS10311, IS35484, IS32841, IS32737, IS39233
Known GenesFGFR3, LETM1, SLBP, TACC3, TMEM129, WHSC1
Method
Analysis
Platform
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)dgv5416n71
Frequency
Sample Size6533
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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