A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2181n54



Internal ID20135605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:108227415..108244860hg38UCSC Ensembl
chr11:108098142..108115587hg19UCSC Ensembl
chr11:107603352..107620797hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3817446
hg1917446
hg1817446
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv556431, nsv556432
Samples
Known GenesATM
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv2181n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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