A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3225592



Internal ID10898572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:9168922..9168975hg38UCSC Ensembl
chr20:9149569..9149622hg19UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7495159
SamplesHuRef
Known GenesPLCB4
MethodSequencing
Analysis
PlatformComplete Genomics
Comments
ReferencePang_et_al_2013b
Pubmed ID24192839
Accession Number(s)esv3225592
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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