A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9663814



Internal ID13452999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:101737007..101737026hg38UCSC Ensembl
Innerchr13:101737003..101737030hg38UCSC Ensembl
Outerchr13:101736984..101737049hg38UCSC Ensembl
chr13:102389357..102389376hg19UCSC Ensembl
Innerchr13:102389353..102389380hg19UCSC Ensembl
Outerchr13:102389334..102389399hg19UCSC Ensembl
chr13:101187358..101187377hg18UCSC Ensembl
Innerchr13:101187381..101187354hg18UCSC Ensembl
Outerchr13:101187335..101187400hg18UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg38300
hg19300
hg18300
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3439313
Supporting Variants
SamplesNA12287
Known GenesFGF14
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv9663814
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