A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12791n54



Internal ID22780686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:89561798..89568281hg38UCSC Ensembl
chr9:92176713..92183196hg19UCSC Ensembl
chr9:91366533..91373016hg18UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg386484
hg196484
hg186484
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv614849, nsv614845, nsv614840
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12791n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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