A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615304



Internal ID16402713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:125746624..125748245hg38UCSC Ensembl
Innerchr9:128508903..128510524hg19UCSC Ensembl
Innerchr9:127548724..127550345hg18UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg381622
hg191622
hg181622
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12867n54
Supporting Variantsnssv1141341, nssv1141340, nssv1141342
Samples
Known GenesPBX3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615304
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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