A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9753952



Internal ID18728198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:33563978..33564266hg38UCSC Ensembl
Outerchr18:33563898..33564292hg38UCSC Ensembl
Innerchr18:31143942..31144230hg19UCSC Ensembl
Outerchr18:31143862..31144256hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg38395
hg19395
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3555205
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9753952
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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