A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12896n54



Internal ID22780791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:129434282..129454751hg38UCSC Ensembl
chr9:132196561..132217030hg19UCSC Ensembl
chr9:131236382..131256851hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3820470
hg1920470
hg1820470
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv615441, nsv615440
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12896n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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