A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv403e199



Internal ID22758176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:75317852..75319282hg38UCSC Ensembl
chr14:75784555..75785985hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg381431
hg191431
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2668243, esv2659719
SamplesNA19700, NA19704, NA19350, NA18486, NA18545, NA19920, NA19373, NA18519, NA19315, NA19904, NA19404, NA18868, NA19235, NA19471, NA18867, NA19451, NA19247, NA19437, NA19455, NA18871, NA18907, NA19114, NA19449, NA19390, NA19435, NA19835, NA19334, NA18501, NA19716, NA18873, NA19463
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv403e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss31
Observed Complex0
Frequencyn/a


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