A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv605e199



Internal ID22758378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:75167884..75176430hg38UCSC Ensembl
chr18:72879839..72888385hg19UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg388547
hg198547
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2658744, esv2671298
SamplesNA19660
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv605e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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