A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9761651



Internal ID18389211
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 StatusS
Merged Variantsesv3562904
Supporting Variants
Samples
Known GenesINADL
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9761651
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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