A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1792n100



Internal ID22787879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:19883118..19957338hg38UCSC Ensembl
chr14:20351277..20425497hg19UCSC Ensembl
chr14:19421117..19495337hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3874221
hg1974221
hg1874221
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1042096, nsv1035401, nsv1035357, nsv1036770
Samples
Known GenesOR4K1, OR4K5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1792n100
Frequency
Sample Size11257
Observed Gain8
Observed Loss0
Observed Complex0
Frequencyn/a


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