A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv619e199



Internal ID22758392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:8269855..8272129hg38UCSC Ensembl
chr19:8334739..8337013hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg382275
hg192275
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2659829, esv2671581
SamplesNA19471
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv619e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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