A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615119



Internal ID16055842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:105772991..105775093hg38UCSC Ensembl
Innerchr9:108535272..108537374hg19UCSC Ensembl
Innerchr9:107575093..107577195hg18UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg382103
hg192103
hg182103
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12837n54
Supporting Variantsnssv1141000
Samples
Known GenesTMEM38B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615119
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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