A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3561821



Internal ID18762897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Cytoband3p21.31
Allele length
AssemblyAllele length
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv293e215
Supporting Variantsessv9760568
Samples
Known GenesSLC6A20
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3561821
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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