A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3556466



Internal ID18757542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:45713971..45714079hg38UCSC Ensembl
Outerchr19:45713963..45714086hg38UCSC Ensembl
Innerchr19:46217229..46217337hg19UCSC Ensembl
Outerchr19:46217221..46217344hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg38124
hg19124
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9755213
Samples
Known GenesFBXO46
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3556466
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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