A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12838n54



Internal ID20146262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:105773891..105775763hg38UCSC Ensembl
chr9:108536172..108538044hg19UCSC Ensembl
chr9:107575993..107577865hg18UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg381873
hg191873
hg181873
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv615121, nsv615125, nsv615132, nsv615126
Samples
Known GenesTMEM38B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12838n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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