A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12038n54



Internal ID22779933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:16604217..16667519hg38UCSC Ensembl
chr8:16461726..16525028hg19UCSC Ensembl
chr8:16506097..16569399hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3863303
hg1963303
hg1863303
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv610667, nsv610666
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12038n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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