A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2140n54



Internal ID22770035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:103158787..103301305hg38UCSC Ensembl
chr11:103029516..103172034hg19UCSC Ensembl
chr11:102534726..102677244hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38142519
hg19142519
hg18142519
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv556171, nsv556172, nsv556173
Samples
Known GenesDYNC2H1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv2140n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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