A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv418e214



Internal ID22756312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:98474082..98575557hg38UCSC Ensembl
chr14:98940419..99041894hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg38101476
hg19101476
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3635464, esv3635463
SamplesNA18628, NA20792
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv418e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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