A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv411e199



Internal ID22758184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:96886417..96897447hg38UCSC Ensembl
chr14:97352754..97363784hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3811031
hg1911031
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2656866, esv2677640
SamplesNA18597, NA18562
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv411e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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