A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1787n100



Internal ID22787874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:19799717..19957689hg38UCSC Ensembl
chr14:20267876..20425848hg19UCSC Ensembl
chr14:19337716..19495688hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38157973
hg19157973
hg18157973
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1050221, nsv1052635, nsv1049564, nsv1053548, nsv1042927
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)dgv1787n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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