A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3642055



Internal ID7028825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:28391870..28396585hg38UCSC Ensembl
Innerchr18:28391878..28396577hg38UCSC Ensembl
Outerchr18:28391862..28396593hg38UCSC Ensembl
chr18:25971834..25976549hg19UCSC Ensembl
Innerchr18:25971842..25976541hg19UCSC Ensembl
Outerchr18:25971826..25976557hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg384716
hg194716
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15829057, essv15829058
SamplesHG02122, HG03084
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3642055
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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