A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7636n54



Internal ID20141060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:61252058..61253165hg38UCSC Ensembl
chr20:59827114..59828221hg19UCSC Ensembl
chr20:59260509..59261616hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg381108
hg191108
hg181108
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv586417, nsv586411, nsv586421, nsv586404, nsv586418, nsv586422, nsv586405, nsv586403
Samples
Known GenesCDH4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7636n54
Frequency
Sample Size17421
Observed Gain26
Observed Loss0
Observed Complex0
Frequencyn/a


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