A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1676e59



Internal ID22762896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:812462..813260hg38UCSC Ensembl
chr17:715702..716500hg19UCSC Ensembl
chr17:662452..663250hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg38799
hg19799
hg18799
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3363833, esv3369458
SamplesNA19239, NA19240
Known GenesNXN
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv1676e59
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