A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1759n54



Internal ID22769654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:41782613..41797430hg38UCSC Ensembl
chr11:41804163..41818980hg19UCSC Ensembl
chr11:41760739..41775556hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3814818
hg1914818
hg1814818
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv554099, nsv554097, nsv554100, nsv554095, nsv554101
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1759n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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