A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12909n54



Internal ID22780804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:130268472..130272119hg38UCSC Ensembl
chr9:133030751..133034398hg19UCSC Ensembl
chr9:132070572..132074219hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg383648
hg193648
hg183648
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv615518, nsv615510, nsv615506, nsv615515, nsv615507, nsv615513, nsv615514, nsv615512, nsv615508, nsv615511, nsv615516, nsv615517, nsv615509
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12909n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss67
Observed Complex0
Frequencyn/a


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