A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1141347



Internal ID15994533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:125747107..125748245hg38UCSC Ensembl
Innerchr9:128509386..128510524hg19UCSC Ensembl
Innerchr9:127549207..127550345hg18UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg381139
hg191139
hg181139
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615307
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)nssv1141347
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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