A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1278n100



Internal ID20152894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:108079845..108178945hg38UCSC Ensembl
chr11:107950572..108049672hg19UCSC Ensembl
chr11:107455782..107554882hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3899101
hg1999101
hg1899101
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1039549, nsv1040522
Samples
Known GenesACAT1, CUL5, NPAT
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1278n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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