A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615139



Internal ID16055862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:105774647..105784157hg38UCSC Ensembl
Innerchr9:108536928..108546438hg19UCSC Ensembl
Innerchr9:107576749..107586259hg18UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg389511
hg199511
hg189511
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1141030
Samples
Known GenesTMEM38B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615139
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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