A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5085n100



Internal ID20156701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:3877879..4208400hg38UCSC Ensembl
chr4:3879606..4210127hg19UCSC Ensembl
chr4:3849404..4261028hg18UCSC Ensembl
Cytoband4p16.2
Allele length
AssemblyAllele length
hg38330522
hg19330522
hg18411625
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1006866, nsv999221, nsv1012590, nsv998283, nsv1005413, nsv1003533, nsv1011861, nsv1015133, nsv1009192, nsv1011749, nsv1007760, nsv998727, nsv1008577, nsv1013710
Samples
Known GenesFAM86EP, OTOP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5085n100
Frequency
Sample Size29084
Observed Gain24
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer