A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3556132



Internal ID18410522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:18131377..18131644hg38UCSC Ensembl
Outerchr19:18131324..18131703hg38UCSC Ensembl
Innerchr19:18242187..18242454hg19UCSC Ensembl
Outerchr19:18242134..18242513hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg38380
hg19380
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9754879
Samples
Known GenesMAST3
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3556132
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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