A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12876n54



Internal ID22780771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:127412817..127423749hg38UCSC Ensembl
chr9:130175096..130186028hg19UCSC Ensembl
chr9:129214917..129225849hg18UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3810933
hg1910933
hg1810933
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv615345, nsv615344
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12876n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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