A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv391e214



Internal ID22756285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:34369096..34374792hg38UCSC Ensembl
chr14:34838302..34843998hg19UCSC Ensembl
Cytoband14q13.1
Allele length
AssemblyAllele length
hg385697
hg195697
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3634026, esv3634027
SamplesNA19334
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv391e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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