A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12214n54



Internal ID22780109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:82407106..82625797hg38UCSC Ensembl
chr8:83319341..83538032hg19UCSC Ensembl
chr8:83481896..83700587hg18UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg38218692
hg19218692
hg18218692
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv611621, nsv611620
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12214n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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