A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7679n54



Internal ID22775574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:63737451..63740688hg38UCSC Ensembl
chr20:62368804..62372041hg19UCSC Ensembl
chr20:61839248..61842485hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg383238
hg193238
hg183238
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv586622, nsv586640, nsv586638, nsv586631, nsv586623, nsv586637, nsv586624
Samples
Known GenesLIME1, SLC2A4RG
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7679n54
Frequency
Sample Size17421
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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