A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7634n54



Internal ID20141058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:61252058..61252852hg38UCSC Ensembl
chr20:59827114..59827908hg19UCSC Ensembl
chr20:59260509..59261303hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38795
hg19795
hg18795
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv586416, nsv586402
Samples
Known GenesCDH4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7634n54
Frequency
Sample Size17421
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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