A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv390e214



Internal ID22756284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:27990251..28053436hg38UCSC Ensembl
chr14:28459457..28522642hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3863186
hg1963186
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3633897, esv3633895
SamplesHG03960, HG03792, HG04001, HG02651, HG04099, HG03681
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv390e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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