A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615135



Internal ID16055858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:105774431..105775421hg38UCSC Ensembl
Innerchr9:108536712..108537702hg19UCSC Ensembl
Innerchr9:107576533..107577523hg18UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg38991
hg19991
hg18991
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12842n54
Supporting Variantsnssv1141022, nssv1141023, nssv1141021
Samples
Known GenesTMEM38B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615135
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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