A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7678n54



Internal ID20141102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:63737451..63739060hg38UCSC Ensembl
chr20:62368804..62370413hg19UCSC Ensembl
chr20:61839248..61840857hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg381610
hg191610
hg181610
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv586627, nsv586619, nsv586620
Samples
Known GenesLIME1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7678n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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