A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3226e59



Internal ID22764446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:14346943..14347441hg38UCSC Ensembl
chr5:14347052..14347550hg19UCSC Ensembl
chr5:14400052..14400550hg18UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg38499
hg19499
hg18499
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3366769, esv3329343
SamplesNA19238, NA19240
Known GenesTRIO
MethodSequencing
Analysis
PlatformIllumina
SOLiD
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv3226e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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