A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1141026



Internal ID15647526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:105774431..105775545hg38UCSC Ensembl
Innerchr9:108536712..108537826hg19UCSC Ensembl
Innerchr9:107576533..107577647hg18UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg381115
hg191115
hg181115
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615136
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)nssv1141026
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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