A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1681e59



Internal ID22762901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:4191308..4192806hg38UCSC Ensembl
chr17:4094603..4096101hg19UCSC Ensembl
chr17:4041352..4042850hg18UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg381499
hg191499
hg181499
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3394792, esv3336734
SamplesNA19238, NA19239
Known GenesANKFY1
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv1681e59
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