A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7620n54



Internal ID20141044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:57525185..57527129hg38UCSC Ensembl
chr20:56100241..56102185hg19UCSC Ensembl
chr20:55533647..55535591hg18UCSC Ensembl
Cytoband20q13.31
Allele length
AssemblyAllele length
hg381945
hg191945
hg181945
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv586317, nsv586320, nsv586338, nsv586326
Samples
Known GenesCTCFL
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7620n54
Frequency
Sample Size17421
Observed Gain20
Observed Loss0
Observed Complex0
Frequencyn/a


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