A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv174e199



Internal ID20123476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:129481108..129487970hg38UCSC Ensembl
chr10:131279372..131286234hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg386863
hg196863
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2663770, esv2659193
SamplesHG01051
Known GenesMGMT
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv174e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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