A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7638n54



Internal ID20141062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:61252058..61257735hg38UCSC Ensembl
chr20:59827114..59832791hg19UCSC Ensembl
chr20:59260509..59266186hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg385678
hg195678
hg185678
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv586427, nsv586408, nsv586415
Samples
Known GenesCDH4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7638n54
Frequency
Sample Size17421
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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