A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1794n100



Internal ID22787881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:19906486..19955201hg38UCSC Ensembl
chr14:20374645..20423360hg19UCSC Ensembl
chr14:19444485..19493200hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3848716
hg1948716
hg1848716
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1046446, nsv1037647, nsv1051708
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)dgv1794n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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