A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv406e214



Internal ID22756300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:70239299..70243323hg38UCSC Ensembl
chr14:70706016..70710040hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg384025
hg194025
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3634854, esv3634856
SamplesHG03687, HG03754, HG03722, HG02505, HG03750, HG04017, HG03778, HG04026, HG03716, HG04056, HG04061
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv406e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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