A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3562904



Internal ID18417294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Cytoband1p31.3
Allele length
AssemblyAllele length
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5e215
Supporting Variantsessv9761651
Samples
Known GenesINADL
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3562904
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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