A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643262



Internal ID7030031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:78420440..78588376hg38UCSC Ensembl
chr18:76180440..76348376hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg38167937
hg19167937
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15951912, essv15951911
SamplesNA21092, NA06984
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643262
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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