A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1753n100



Internal ID20153369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:18225635..19959442hg38UCSC Ensembl
chr14:19002112..20427601hg19UCSC Ensembl
chr14:18072112..19497441hg18UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg381733808
hg191425490
hg181425330
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1044774, nsv1048983, nsv1036227, nsv1052617, nsv1045786, nsv1051271, nsv1048472, nsv1052494, nsv1041724, nsv1035643, nsv1037840, nsv1040399, nsv1041056, nsv1053315, nsv1045206, nsv1047691, nsv1044749, nsv1040493, nsv1054438, nsv1043211, nsv1048306
Samples
Known GenesBMS1P17, BMS1P18, LOC642426, OR11H12, OR11H2, OR4K1, OR4K2, OR4K5, OR4M1, OR4N2, OR4Q3, POTEG, POTEM
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1753n100
Frequency
Sample Size29084
Observed Gain64
Observed Loss0
Observed Complex0
Frequencyn/a


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