A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1659n54



Internal ID18993835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:13277469..13278110hg38UCSC Ensembl
chr11:13299016..13299657hg19UCSC Ensembl
chr11:13255592..13256233hg18UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg38642
hg19642
hg18642
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv553553, nsv553555
Samples
Known GenesARNTL
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1659n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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