A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2833792



Internal ID10853489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:133784927..133786243hg38UCSC Ensembl
Outerchr3:133503771..133505087hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg381317
hg191317
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7103359
SamplesHuRef
Known GenesSRPRB
MethodSequencing
Analysis
PlatformComplete Genomics
Comments
ReferencePang_et_al_2013b
Pubmed ID24192839
Accession Number(s)esv2833792
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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