A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1205n100



Internal ID22787292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:55693312..56247291hg38UCSC Ensembl
chr11:55460788..56014767hg19UCSC Ensembl
chr11:55217364..55771343hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38553980
hg19553980
hg18553980
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1043441, nsv1036666, nsv1049004
Samples
Known GenesOR10AG1, OR5AS1, OR5D13, OR5D14, OR5D16, OR5D18, OR5F1, OR5I1, OR5J2, OR5L1, OR5L2, OR5T2, OR5W2, OR7E5P, OR8H2, OR8H3, OR8I2, OR8J3, OR8K5, TRIM51
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1205n100
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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