A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv171e199



Internal ID22757944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:121010132..121029479hg38UCSC Ensembl
chr10:122769645..122788992hg19UCSC Ensembl
Cytoband10q26.12
Allele length
AssemblyAllele length
hg3819348
hg1919348
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2658667, esv2672582, esv2662007
SamplesNA19394, NA19700, NA18924, NA19359, NA18870, NA19171, NA19379, NA19131, NA18916, NA19197, NA18874, NA19172, NA19317, NA19901, NA19189, NA20342, NA20127, NA18867, NA19451, NA19247, NA19707, NA19403, NA18933, NA19391, NA19327, NA18516, NA19449, HG01101, NA18853, NA20282, NA19099, NA19338, NA19257, NA19452, NA19318, NA18909, NA19108, NA19256, NA19712, NA19434, HG00638, NA19444, NA19835, NA19467, NA20281, NA19818, NA19248, NA19102, NA18511, NA19429, NA18487
Known GenesMIR5694
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv171e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss51
Observed Complex0
Frequencyn/a


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