A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3556398



Internal ID18757474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:40647449..40649873hg38UCSC Ensembl
Outerchr19:40647303..40650226hg38UCSC Ensembl
Innerchr19:41153354..41155778hg19UCSC Ensembl
Outerchr19:41153208..41156131hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg382924
hg192924
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9755145
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3556398
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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