A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3563493



Internal ID18764569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:67542321..67543125hg38UCSC Ensembl
Outerchr1:67542141..67543197hg38UCSC Ensembl
Innerchr1:68008004..68008808hg19UCSC Ensembl
Outerchr1:68007824..68008880hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg381057
hg191057
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9762240
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3563493
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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