A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1193n100



Internal ID22787280
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:55609010..55836203hg38UCSC Ensembl
chr11:55376486..55603679hg19UCSC Ensembl
chr11:55133062..55360255hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38227194
hg19227194
hg18227194
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1051510, nsv1036940
Samples
Known GenesOR4C6, OR4P4, OR4S2, OR5D13, OR5D14, OR5D18, OR5L1, OR5L2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1193n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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