A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3555184



Internal ID18756260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:30115057..30115482hg38UCSC Ensembl
Outerchr18:30115039..30115523hg38UCSC Ensembl
Innerchr18:27695022..27695447hg19UCSC Ensembl
Outerchr18:27695004..27695488hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg38485
hg19485
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9753931
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3555184
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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