A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615131



Internal ID16055854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:105774230..105775421hg38UCSC Ensembl
Innerchr9:108536511..108537702hg19UCSC Ensembl
Innerchr9:107576332..107577523hg18UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg381192
hg191192
hg181192
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12842n54
Supporting Variantsnssv1141016, nssv1141015
Samples
Known GenesTMEM38B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615131
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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