A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3555292



Internal ID18756368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:43873497..43873790hg38UCSC Ensembl
Outerchr18:43873430..43873825hg38UCSC Ensembl
Innerchr18:41453462..41453755hg19UCSC Ensembl
Outerchr18:41453395..41453790hg19UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg38396
hg19396
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9754039
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3555292
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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