A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv422e214



Internal ID18980597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:103355152..103437655hg38UCSC Ensembl
chr14:103821489..103903992hg19UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg3882504
hg1982504
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3635593, esv3635591
SamplesNA12341, NA06984, HG00598
Known GenesMARK3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv422e214
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer