A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv399e214



Internal ID22756293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:46513876..46528583hg38UCSC Ensembl
chr14:46983079..46997786hg19UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg3814708
hg1914708
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3634390, esv3634389
SamplesNA20581
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv399e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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