A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1524n54



Internal ID20134948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:610277..619789hg38UCSC Ensembl
chr11:610277..619789hg19UCSC Ensembl
chr11:600277..609789hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg389513
hg199513
hg189513
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv552864, nsv552863
Samples
Known GenesCDHR5, IRF7, PHRF1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1524n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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