A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12742n54



Internal ID22780637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:69280692..69284053hg38UCSC Ensembl
chr9:71895608..71898969hg19UCSC Ensembl
chr9:71085428..71088789hg18UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg383362
hg193362
hg183362
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv614562, nsv614563
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12742n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss14
Observed Complex0
Frequencyn/a


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