A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15829089



Internal ID5826805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:28393592..28396130hg38UCSC Ensembl
Innerchr18:28393604..28396118hg38UCSC Ensembl
Outerchr18:28393580..28396142hg38UCSC Ensembl
chr18:25973556..25976094hg19UCSC Ensembl
Innerchr18:25973568..25976082hg19UCSC Ensembl
Outerchr18:25973544..25976106hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg382539
hg192539
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3642056
Supporting Variants
SamplesNA19204
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15829089
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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