A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615299



Internal ID16402708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:125746419..125748039hg38UCSC Ensembl
Innerchr9:128508698..128510318hg19UCSC Ensembl
Innerchr9:127548519..127550139hg18UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg381621
hg191621
hg181621
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12867n54
Supporting Variantsnssv1141326
Samples
Known GenesPBX3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615299
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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