A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9753771



Internal ID18728017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:8934744..8934846hg38UCSC Ensembl
chr18:8934742..8934844hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg38103
hg19103
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3555024
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9753771
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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