A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3642066



Internal ID7028836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:28721273..28768553hg38UCSC Ensembl
Innerchr18:28721273..28768553hg38UCSC Ensembl
Outerchr18:28720773..28769053hg38UCSC Ensembl
chr18:26301237..26348517hg19UCSC Ensembl
Innerchr18:26301237..26348517hg19UCSC Ensembl
Outerchr18:26300737..26349017hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg3847281
hg1947281
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15830577
SamplesHG03485
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3642066
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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