A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1236n100



Internal ID22787323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:80256492..80274585hg38UCSC Ensembl
chr11:79967536..79985629hg19UCSC Ensembl
chr11:79645184..79663277hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3818094
hg1918094
hg1818094
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1035946, nsv1053741, nsv1038070, nsv1052871, nsv1041610, nsv1055057, nsv1046524
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)dgv1236n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss19
Observed Complex0
Frequencyn/a


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