A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12057n54



Internal ID20145481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:23071837..23183569hg38UCSC Ensembl
chr8:22929350..23041082hg19UCSC Ensembl
chr8:22985295..23097027hg18UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg38111733
hg19111733
hg18111733
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv610776, nsv610774
Samples
Known GenesLOC254896, LOC286059, TNFRSF10C, TNFRSF10D
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12057n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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