A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615126



Internal ID16055849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:105773926..105775763hg38UCSC Ensembl
Innerchr9:108536207..108538044hg19UCSC Ensembl
Innerchr9:107576028..107577865hg18UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg381838
hg191838
hg181838
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12838n54
Supporting Variantsnssv1141009
Samples
Known GenesTMEM38B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615126
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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