A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1890n100



Internal ID22787977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:43275491..43779976hg38UCSC Ensembl
chr14:43744694..44249179hg19UCSC Ensembl
chr14:42814444..43318929hg18UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg38504486
hg19504486
hg18504486
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1040702, nsv1038437, nsv1045856, nsv1041159, nsv1038363, nsv1052435, nsv1045487, nsv1051846, nsv1042385, nsv1045208, nsv1036295, nsv1037286, nsv1042031, nsv1054494, nsv1052296
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1890n100
Frequency
Sample Size11257
Observed Gain37
Observed Loss0
Observed Complex0
Frequencyn/a


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