A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1155n100



Internal ID22787242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:54554865..54941169hg38UCSC Ensembl
chr11:51176562..51564415hg19UCSC Ensembl
chr11:51033138..51420991hg18UCSC Ensembl
Cytoband11p11.11
Allele length
AssemblyAllele length
hg38386305
hg19387854
hg18387854
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1051064, nsv1048401, nsv1040974, nsv1044063, nsv1045774, nsv1036334, nsv1046059, nsv1054282, nsv1036886
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)dgv1155n100
Frequency
Sample Size11257
Observed Gain16
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer