A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3555392



Internal ID18409782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:52481273..52481405hg38UCSC Ensembl
Outerchr18:52481268..52481409hg38UCSC Ensembl
Innerchr18:50007643..50007775hg19UCSC Ensembl
Outerchr18:50007638..50007779hg19UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg38142
hg19142
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9754139
Samples
Known GenesDCC
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3555392
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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