A curated catalogue of human genomic structural variation




Variant Details

Variant: esv33660



Internal ID1683009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:64257169..64258705hg19UCSC Ensembl
Innerchr10:63927175..63928711hg18UCSC Ensembl
Innerchr10:63927175..63928711hg17UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg191899
hg181899
hg171899
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsessv98091
Samples22259
Known GenesZNF365
Method
Analysis
PlatformAgilent-015366 Custom Human 244K CGH Microarray
Comments
Referencede_Smith_et_al_2007
Pubmed ID17666407
Accession Number(s)esv33660
Frequency
Sample Size51
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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