A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1160n100



Internal ID22787247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:54953335..55208953hg38UCSC Ensembl
chr11:54720811..54976429hg19UCSC Ensembl
chr11:54477387..54733005hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38255619
hg19255619
hg18255619
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1049068, nsv1043503, nsv1049385, nsv1053153
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1160n100
Frequency
Sample Size11257
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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