A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3303654



Internal ID15150602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:10308863..10308864hg38UCSC Ensembl
Innerchr18:10308832..10308895hg38UCSC Ensembl
Outerchr18:10308831..10308896hg38UCSC Ensembl
chr18:10308860..10308861hg19UCSC Ensembl
Innerchr18:10308829..10308892hg19UCSC Ensembl
Outerchr18:10308828..10308893hg19UCSC Ensembl
chr18:10298860..10298861hg18UCSC Ensembl
Innerchr18:10298892..10298829hg18UCSC Ensembl
Outerchr18:10298828..10298893hg18UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg38120
hg19120
hg18120
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7760356, essv7763213, essv7746752, essv7756219, essv7742336, essv7755216, essv7758778
SamplesNA18870, NA18519, NA19138, NA18907, NA18523, NA19116, NA19129
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3303654
Frequency
Sample Size185
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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