A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1624n54



Internal ID22769519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:6094808..6100320hg38UCSC Ensembl
chr11:6116038..6121550hg19UCSC Ensembl
chr11:6072614..6078126hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg385513
hg195513
hg185513
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv553363, nsv553361, nsv553359, nsv553367, nsv553358, nsv553355, nsv553356, nsv553364, nsv553357, nsv553368, nsv553362, nsv553365, nsv553360, nsv553369
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1624n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss19
Observed Complex0
Frequencyn/a


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