A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1786n100



Internal ID22787873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:19791588..19955201hg38UCSC Ensembl
chr14:20259747..20423360hg19UCSC Ensembl
chr14:19329587..19493200hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38163614
hg19163614
hg18163614
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1039428, nsv1044561, nsv1035507, nsv1049775, nsv1046600, nsv1038751, nsv1043151, nsv1041031, nsv1036813
Samples
Known GenesOR4K1, OR4K2, OR4K5, OR4N2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1786n100
Frequency
Sample Size11257
Observed Gain11
Observed Loss0
Observed Complex0
Frequencyn/a


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