A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2056n54



Internal ID22769951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:87217211..87290850hg38UCSC Ensembl
chr11:86928253..87001892hg19UCSC Ensembl
chr11:86605901..86679540hg18UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg3873640
hg1973640
hg1873640
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv555709, nsv555710
Samples
Known GenesTMEM135
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv2056n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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