A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv170e199



Internal ID22757943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:113447601..113457214hg38UCSC Ensembl
chr10:115207360..115216973hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg389614
hg199614
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2672978, esv2671420
SamplesNA20508, NA12045, HG00136
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv170e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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