A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1173n100



Internal ID20152789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:55574203..55672502hg38UCSC Ensembl
chr11:55341679..55439978hg19UCSC Ensembl
chr11:55098255..55196554hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3898300
hg1998300
hg1898300
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1048385, nsv1053146, nsv1044343, nsv1044485, nsv1045845, nsv1037084, nsv1054864, nsv1053726, nsv1051928, nsv1054704, nsv1044066, nsv1052210
Samples
Known GenesOR4C11, OR4C6, OR4P4, OR4S2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1173n100
Frequency
Sample Size29084
Observed Gain19
Observed Loss0
Observed Complex0
Frequencyn/a


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