A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1747n54



Internal ID22769642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:37923359..37985098hg38UCSC Ensembl
chr11:37944909..38006648hg19UCSC Ensembl
chr11:37901485..37963224hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3861740
hg1961740
hg1861740
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv554022, nsv554021
Samples1798860114_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1747n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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