A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1280n100



Internal ID22787367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:115973204..116000455hg38UCSC Ensembl
chr11:115843922..115871173hg19UCSC Ensembl
chr11:115349132..115376383hg18UCSC Ensembl
Cytoband11q23.2
Allele length
AssemblyAllele length
hg3827252
hg1927252
hg1827252
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1052695, nsv1051105
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)dgv1280n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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