A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2135n54



Internal ID22770030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:102434334..102436612hg38UCSC Ensembl
chr11:102305065..102307343hg19UCSC Ensembl
chr11:101810275..101812553hg18UCSC Ensembl
Cytoband11q22.2
Allele length
AssemblyAllele length
hg382279
hg192279
hg182279
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv556148, nsv556147, nsv556149
Samples
Known GenesTMEM123
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv2135n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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