A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3555896



Internal ID18410286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Cytoband19p13.3
Allele length
AssemblyAllele length
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv216e215
Supporting Variantsessv9754643
Samples
Known GenesANKRD24
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3555896
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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