A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv861e199



Internal ID22758634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:47482589..47491753hg38UCSC Ensembl
chr3:47524079..47533243hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg389165
hg199165
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2664959, esv2660973, esv2677034
SamplesNA19448, NA19445, NA19346
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv861e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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