A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1751n54



Internal ID22769646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:38227656..38379666hg38UCSC Ensembl
chr11:38249206..38401216hg19UCSC Ensembl
chr11:38205782..38357792hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38152011
hg19152011
hg18152011
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv554039, nsv554047, nsv554038, nsv554052
SamplesNINDS_183
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1751n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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