A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3559759



Internal ID18760835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:36108517..36108568hg38UCSC Ensembl
chr19:36599419..36599470hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv222e215
Supporting Variantsessv9758506
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3559759
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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