A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3556063



Internal ID18757139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:13664919..13666036hg38UCSC Ensembl
Outerchr19:13664737..13666117hg38UCSC Ensembl
Innerchr19:13775733..13776850hg19UCSC Ensembl
Outerchr19:13775551..13776931hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg381381
hg191381
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv218e215
Supporting Variantsessv9754810
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3556063
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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