A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1913n100



Internal ID22788000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:47358234..47411757hg38UCSC Ensembl
chr14:47827437..47880960hg19UCSC Ensembl
chr14:46897187..46950710hg18UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg3853524
hg1953524
hg1853524
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1037655, nsv1053559
Samples
Known GenesMDGA2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1913n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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