A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3555212



Internal ID18756288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:34166770..34167064hg38UCSC Ensembl
Outerchr18:34166685..34167122hg38UCSC Ensembl
Innerchr18:31746734..31747028hg19UCSC Ensembl
Outerchr18:31746649..31747086hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg38438
hg19438
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9753959
Samples
Known GenesNOL4
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3555212
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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