A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv839e199



Internal ID20124141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:49954677..49960250hg38UCSC Ensembl
chr22:50348325..50353898hg19UCSC Ensembl
Cytoband22q13.33
Allele length
AssemblyAllele length
hg385574
hg195574
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2673502, esv2661343
SamplesNA18616
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv839e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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