A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv134e199



Internal ID22757907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:42888832..42892217hg38UCSC Ensembl
chr10:43384280..43387665hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg383386
hg193386
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2661403, esv2665936
SamplesNA18867
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv134e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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