A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615306



Internal ID16402715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:125746624..125766699hg38UCSC Ensembl
Innerchr9:128508903..128528978hg19UCSC Ensembl
Innerchr9:127548724..127568799hg18UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3820076
hg1920076
hg1820076
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1141346
Samples
Known GenesPBX3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615306
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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