A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3555806



Internal ID18410196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:323213..323368hg38UCSC Ensembl
Outerchr19:323199..323381hg38UCSC Ensembl
Innerchr19:323213..323368hg19UCSC Ensembl
Outerchr19:323199..323381hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38183
hg19183
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9754553
Samples
Known GenesMIER2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3555806
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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