A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615128



Internal ID16055851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:105774028..105775194hg38UCSC Ensembl
Innerchr9:108536309..108537475hg19UCSC Ensembl
Innerchr9:107576130..107577296hg18UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg381167
hg191167
hg181167
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12840n54
Supporting Variantsnssv1141011
Samples
Known GenesTMEM38B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615128
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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