A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv11988n54



Internal ID22779883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:12865194..12916449hg38UCSC Ensembl
chr8:12722703..12773958hg19UCSC Ensembl
chr8:12767074..12818329hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3851256
hg1951256
hg1851256
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv610407, nsv610408
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv11988n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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