A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12520n54



Internal ID22780415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:10657520..10688795hg38UCSC Ensembl
chr9:10657520..10688795hg19UCSC Ensembl
chr9:10647520..10678795hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3831276
hg1931276
hg1831276
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv613398, nsv613400, nsv613399, nsv613401, nsv613397, nsv613396, nsv613402
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12520n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


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