A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7681n54



Internal ID20141105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:63737667..63739379hg38UCSC Ensembl
chr20:62369020..62370732hg19UCSC Ensembl
chr20:61839464..61841176hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg381713
hg191713
hg181713
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv586639, nsv586628, nsv586635
Samples
Known GenesLIME1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7681n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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