A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12842n54



Internal ID20146266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:105774230..105775763hg38UCSC Ensembl
chr9:108536511..108538044hg19UCSC Ensembl
chr9:107576332..107577865hg18UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg381534
hg191534
hg181534
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv615135, nsv615131, nsv615137
Samples
Known GenesTMEM38B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12842n54
Frequency
Sample Size17421
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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