A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3352453



Internal ID14852717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:40563915..40566013hg38UCSC Ensembl
Innerchr13:40564915..40565013hg38UCSC Ensembl
Outerchr13:40562915..40567013hg38UCSC Ensembl
chr13:41138052..41140150hg19UCSC Ensembl
Innerchr13:41139052..41139150hg19UCSC Ensembl
Outerchr13:41137052..41141150hg19UCSC Ensembl
chr13:40036052..40038150hg18UCSC Ensembl
Innerchr13:40037052..40037150hg18UCSC Ensembl
Outerchr13:40035052..40039150hg18UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg382099
hg192099
hg182099
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8688948
SamplesNA19239
Known GenesFOXO1
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3352453
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