A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9751145



Internal ID18725391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Cytoband15q21.1
Allele length
AssemblyAllele length
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3552398
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9751145
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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