A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3555042



Internal ID18756118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:10150606..10150995hg38UCSC Ensembl
Outerchr18:10150543..10151046hg38UCSC Ensembl
Innerchr18:10150603..10150992hg19UCSC Ensembl
Outerchr18:10150540..10151043hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg38504
hg19504
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9753789
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3555042
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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