A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2673421



Internal ID9939526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:15616189..15674477hg38UCSC Ensembl
chr19:15727000..15785287hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3858289
hg1958288
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv627e199
Supporting Variantsessv5731420
SamplesHG00245
Known GenesCYP4F12, CYP4F3, CYP4F8
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2673421
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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