A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3556193



Internal ID18757269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:22652223..22652382hg38UCSC Ensembl
Outerchr19:22652221..22652388hg38UCSC Ensembl
Innerchr19:22835025..22835184hg19UCSC Ensembl
Outerchr19:22835023..22835190hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38168
hg19168
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9754940
Samples
Known GenesZNF492
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3556193
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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