A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8697308



Internal ID15104355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:65262026..65282724hg38UCSC Ensembl
Innerchr9:65263026..65281724hg38UCSC Ensembl
Outerchr9:65261026..65283724hg38UCSC Ensembl
chr9:70155632..70176330hg19UCSC Ensembl
Innerchr9:70156632..70175330hg19UCSC Ensembl
Outerchr9:70154632..70177330hg19UCSC Ensembl
chr9:69445452..69466150hg18UCSC Ensembl
Innerchr9:69446452..69465150hg18UCSC Ensembl
Outerchr9:69444452..69467150hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg3820699
hg1920699
hg1820699
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag0
Merged StatusS
Merged Variantsesv3446735
Supporting Variants
SamplesNA19240
Known GenesFOXD4L5
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8697308
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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