A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12786n54



Internal ID22780681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:88534103..88535071hg38UCSC Ensembl
chr9:91149018..91149986hg19UCSC Ensembl
chr9:90338838..90339806hg18UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg38969
hg19969
hg18969
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv614816, nsv614819, nsv614811, nsv614815, nsv614813, nsv614817, nsv614810
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12786n54
Frequency
Sample Size17421
Observed Gain45
Observed Loss0
Observed Complex0
Frequencyn/a


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