A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3642014



Internal ID6682095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:26040304..26045872hg38UCSC Ensembl
Innerchr18:26040304..26045872hg38UCSC Ensembl
Outerchr18:26039804..26046372hg38UCSC Ensembl
chr18:23620268..23625836hg19UCSC Ensembl
Innerchr18:23620268..23625836hg19UCSC Ensembl
Outerchr18:23619768..23626336hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg385569
hg195569
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15822117
SamplesNA12815
Known GenesSS18
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3642014
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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