A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9753994



Internal ID18728240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:37735698..37735960hg38UCSC Ensembl
Outerchr18:37735634..37735992hg38UCSC Ensembl
Innerchr18:35315661..35315923hg19UCSC Ensembl
Outerchr18:35315597..35315955hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg38359
hg19359
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3555247
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9753994
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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