A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5418n71



Internal ID6323038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:1785738..1809787hg19UCSC Ensembl
chr4:1755536..1779585hg18UCSC 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 Variantsnsv878411, nsv878409, nsv878407, nsv878412, nsv878410, nsv878408, nsv878406
SamplesSP54043, SP54225, SP55056, SP81010, SP54782, SP56223, SP54593, SP55992, SP51109
Known GenesFGFR3
Method
Analysis
Platform
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)dgv5418n71
Frequency
Sample Size6533
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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