A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12614n54



Internal ID22780509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:25562456..25599997hg38UCSC Ensembl
chr9:25562454..25599995hg19UCSC Ensembl
chr9:25552454..25589995hg18UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg3837542
hg1937542
hg1837542
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv613915, nsv613914
SamplesHGDP00267, NINDS_213, NINDS_156
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12614n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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