A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3555936



Internal ID18410326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:5810076..5810670hg38UCSC Ensembl
Outerchr19:5810002..5810832hg38UCSC Ensembl
Innerchr19:5810087..5810681hg19UCSC Ensembl
Outerchr19:5810013..5810843hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38831
hg19831
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9754683
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3555936
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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