A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3555876



Internal ID18410266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:3310043..3310095hg38UCSC Ensembl
Outerchr19:3310039..3310098hg38UCSC Ensembl
Innerchr19:3310041..3310093hg19UCSC Ensembl
Outerchr19:3310037..3310096hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9754623
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3555876
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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