A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1157n100



Internal ID22787244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:54554865..54782218hg38UCSC Ensembl
chr11:51337062..51564415hg19UCSC Ensembl
chr11:51193638..51420991hg18UCSC Ensembl
Cytoband11p11.11
Allele length
AssemblyAllele length
hg38227354
hg19227354
hg18227354
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1048422, nsv1041340, nsv1048850
Samples
Known GenesOR4A5, OR4C46
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1157n100
Frequency
Sample Size11257
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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