A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2057n54



Internal ID22769952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:87249474..87302396hg38UCSC Ensembl
chr11:86960516..87013438hg19UCSC Ensembl
chr11:86638164..86691086hg18UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg3852923
hg1952923
hg1852923
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv555712, nsv555711, nsv555713
Samples
Known GenesTMEM135
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv2057n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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