A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1789n100



Internal ID22787876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:19831403..19957689hg38UCSC Ensembl
chr14:20299562..20425848hg19UCSC Ensembl
chr14:19369402..19495688hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38126287
hg19126287
hg18126287
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1037265, nsv1047681, nsv1037192, nsv1039616
Samples
Known GenesOR4K1, OR4K2, OR4K5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1789n100
Frequency
Sample Size11257
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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