A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv494e199



Internal ID22758267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:46395183..46465185hg38UCSC Ensembl
chr16:46429095..46499097hg19UCSC Ensembl
Cytoband16q11.2
Allele length
AssemblyAllele length
hg3870003
hg1970003
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2676805, esv2668607, esv2661622
SamplesHG01070, NA19764, NA19473, HG01061
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv494e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer