A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv116e199



Internal ID20123418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:8020025..8026173hg38UCSC Ensembl
chr10:8061988..8068136hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg386149
hg196149
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2669845, esv2662807
SamplesHG00345
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv116e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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