A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12841n54



Internal ID20146265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:105774230..105775545hg38UCSC Ensembl
chr9:108536511..108537826hg19UCSC Ensembl
chr9:107576332..107577647hg18UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg381316
hg191316
hg181316
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv615130, nsv615136
Samples
Known GenesTMEM38B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12841n54
Frequency
Sample Size17421
Observed Gain4
Observed Loss2
Observed Complex0
Frequencyn/a


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