A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12837n54



Internal ID20146261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:105772991..105775421hg38UCSC Ensembl
chr9:108535272..108537702hg19UCSC Ensembl
chr9:107575093..107577523hg18UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg382431
hg192431
hg182431
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv615120, nsv615118, nsv615119
Samples
Known GenesTMEM38B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12837n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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