A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7635n54



Internal ID20141059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:61252058..61253059hg38UCSC Ensembl
chr20:59827114..59828115hg19UCSC Ensembl
chr20:59260509..59261510hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg381002
hg191002
hg181002
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv586401, nsv586409, nsv586410
Samples
Known GenesCDH4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7635n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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