A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3556089



Internal ID18757165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:15651163..15651539hg38UCSC Ensembl
Outerchr19:15651119..15651640hg38UCSC Ensembl
Innerchr19:15761973..15762349hg19UCSC Ensembl
Outerchr19:15761929..15762450hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg38522
hg19522
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9754836
Samples
Known GenesCYP4F3
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3556089
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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