A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3555126



Internal ID18409516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:21710279..21710688hg38UCSC Ensembl
Outerchr18:21710268..21710697hg38UCSC Ensembl
Innerchr18:19290240..19290649hg19UCSC Ensembl
Outerchr18:19290229..19290658hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38430
hg19430
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9753873
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3555126
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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