A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1141328



Internal ID15994514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:125746419..125748317hg38UCSC Ensembl
Innerchr9:128508698..128510596hg19UCSC Ensembl
Innerchr9:127548519..127550417hg18UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg381899
hg191899
hg181899
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615300
Supporting Variants
Samples
Known GenesPBX3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1141328
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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