A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3555405



Internal ID18756481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:53399626..53399925hg38UCSC Ensembl
Outerchr18:53399582..53399966hg38UCSC Ensembl
Innerchr18:50925996..50926295hg19UCSC Ensembl
Outerchr18:50925952..50926336hg19UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg38385
hg19385
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9754152
Samples
Known GenesDCC
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3555405
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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