A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1760n54



Internal ID22769655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:41782613..41806798hg38UCSC Ensembl
chr11:41804163..41828348hg19UCSC Ensembl
chr11:41760739..41784924hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3824186
hg1924186
hg1824186
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv554096, nsv554098
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1760n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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