A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3556049



Internal ID18410439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:12642682..12643680hg38UCSC Ensembl
Outerchr19:12642454..12643864hg38UCSC Ensembl
Innerchr19:12753496..12754494hg19UCSC Ensembl
Outerchr19:12753268..12754678hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg381411
hg191411
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9754796
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3556049
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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