A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9681036



Internal ID14911920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:35631620..35631639hg38UCSC Ensembl
Innerchr22:35631616..35631643hg38UCSC Ensembl
Outerchr22:35631597..35631662hg38UCSC Ensembl
chr22:36027667..36027686hg19UCSC Ensembl
Innerchr22:36027663..36027690hg19UCSC Ensembl
Outerchr22:36027644..36027709hg19UCSC Ensembl
chr22:34357613..34357632hg18UCSC Ensembl
Innerchr22:34357636..34357609hg18UCSC Ensembl
Outerchr22:34357590..34357655hg18UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38300
hg19300
hg18300
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3428009
Supporting Variants
SamplesNA19143
Known Genes
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv9681036
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