A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1168n100



Internal ID19011536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:55262739..55380687hg38UCSC Ensembl
chr11:55030215..55148163hg19UCSC Ensembl
chr11:54786791..54904739hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38117949
hg19117949
hg18117949
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1054262, nsv1050431
Samples
Known GenesOR4A15, OR4A16, TRIM48, TRIM51HP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1168n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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