A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1226n100



Internal ID20152842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:76158391..76198575hg38UCSC Ensembl
chr11:75869435..75909619hg19UCSC Ensembl
chr11:75547083..75587267hg18UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg3840185
hg1940185
hg1840185
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1038104, nsv1044348, nsv1037453, nsv1040591, nsv1041667, nsv1045109, nsv1043964, nsv1045854, nsv1047833, nsv1053291, nsv1053580
Samples
Known GenesWNT11
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1226n100
Frequency
Sample Size29084
Observed Gain23
Observed Loss0
Observed Complex0
Frequencyn/a


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