A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1306n100



Internal ID20152922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:134373155..134500539hg38UCSC Ensembl
chr11:134243049..134370433hg19UCSC Ensembl
chr11:133748259..133875643hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38127385
hg19127385
hg18127385
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1046344, nsv1044424, nsv1044328
Samples
Known GenesB3GAT1, GLB1L2, LOC283177
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1306n100
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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