A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12467n54



Internal ID22780362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:2012767..2066493hg38UCSC Ensembl
chr9:2012767..2066493hg19UCSC Ensembl
chr9:2002767..2056493hg18UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg3853727
hg1953727
hg1853727
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv613080, nsv613079
Samples1780862414_A
Known GenesSMARCA2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12467n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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