A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615136



Internal ID16055859
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+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12841n54
Supporting Variantsnssv1141025, nssv1141027, nssv1141026, nssv1141024
Samples
Known GenesTMEM38B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615136
Frequency
Sample Size17421
Observed Gain3
Observed Loss1
Observed Complex0
Frequencyn/a


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