A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12618n54



Internal ID22780513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:26265881..26423084hg38UCSC Ensembl
chr9:26265879..26423082hg19UCSC Ensembl
chr9:26255879..26413082hg18UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg38157204
hg19157204
hg18157204
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv613933, nsv613934, nsv613935, nsv613936
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12618n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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