A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1790n100



Internal ID22787877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:19869145..19955201hg38UCSC Ensembl
chr14:20337304..20423360hg19UCSC Ensembl
chr14:19407144..19493200hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3886057
hg1986057
hg1886057
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1052037, nsv1054798, nsv1054721, nsv1041442, nsv1052976
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)dgv1790n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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