A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1163n100



Internal ID22787250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:54953335..55293044hg38UCSC Ensembl
chr11:54720811..55060520hg19UCSC Ensembl
chr11:54477387..54817096hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38339710
hg19339710
hg18339710
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1045259, nsv1052399, nsv1044556, nsv1048711
Samples
Known GenesTRIM48
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1163n100
Frequency
Sample Size11257
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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