A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1667n54



Internal ID22769562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:18074268..18079252hg38UCSC Ensembl
chr11:18095815..18100799hg19UCSC Ensembl
chr11:18052391..18057375hg18UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg384985
hg194985
hg184985
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv553594, nsv553593, nsv553592
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1667n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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