A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3556031



Internal ID18410421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:11439822..11440660hg38UCSC Ensembl
Outerchr19:11439779..11440704hg38UCSC Ensembl
Innerchr19:11550636..11551475hg19UCSC Ensembl
Outerchr19:11550593..11551519hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38926
hg19927
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9754778
Samples
Known GenesPRKCSH
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3556031
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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