A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2139n54



Internal ID22770034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:103118231..103185951hg38UCSC Ensembl
chr11:102988960..103056680hg19UCSC Ensembl
chr11:102494170..102561890hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3867721
hg1967721
hg1867721
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv556167, nsv556168
SamplesHGDP01061
Known GenesDYNC2H1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv2139n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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