A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1778n100



Internal ID22787865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:19732012..19959442hg38UCSC Ensembl
chr14:20200171..20427601hg19UCSC Ensembl
chr14:19270011..19497441hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38227431
hg19227431
hg18227431
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1051529, nsv1041082, nsv1054715, nsv1054251, nsv1049522, nsv1047706, nsv1048927, nsv1045848, nsv1043777, nsv1036405, nsv1044350, nsv1038720, nsv1051690, nsv1046844, nsv1048111, nsv1041479, nsv1050120, nsv1043760, nsv1052042, nsv1043676, nsv1039400, nsv1038171, nsv1044045, nsv1046255, nsv1054368, nsv1044013, nsv1047940, nsv1049233, nsv1052302, nsv1042299, nsv1049755, nsv1039759, nsv1054316, nsv1039664, nsv1037191, nsv1046795, nsv1039396, nsv1039335, nsv1036244, nsv1047679, nsv1054964, nsv1049290, nsv1047396, nsv1044423, nsv1035666
Samples
Known GenesOR4K1, OR4K2, OR4K5, OR4M1, OR4N2, OR4Q3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1778n100
Frequency
Sample Size11257
Observed Gain562
Observed Loss0
Observed Complex0
Frequencyn/a


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