A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12840n54



Internal ID20146264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:105773926..105775245hg38UCSC Ensembl
chr9:108536207..108537526hg19UCSC Ensembl
chr9:107576028..107577347hg18UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg381320
hg191320
hg181320
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv615128, nsv615129, nsv615124
Samples
Known GenesTMEM38B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12840n54
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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