A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7676n54



Internal ID18999852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:63686867..63702868hg38UCSC Ensembl
chr20:62318220..62334220hg19UCSC Ensembl
chr20:61788664..61804664hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3816002
hg1916001
hg1816001
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv586613, nsv586612
Samples
Known GenesARFRP1, RTEL1, RTEL1-TNFRSF6B, TNFRSF6B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7676n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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