A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1141012



Internal ID15647512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:105774230..105775194hg38UCSC Ensembl
Innerchr9:108536511..108537475hg19UCSC Ensembl
Innerchr9:107576332..107577296hg18UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg38965
hg19965
hg18965
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615129
Supporting Variants
Samples
Known GenesTMEM38B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1141012
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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