A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3451275



Internal ID15298222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:6678632..6679068hg38UCSC Ensembl
Innerchr8:6678632..6679068hg38UCSC Ensembl
Outerchr8:6677933..6679305hg38UCSC Ensembl
chr8:6536153..6536589hg19UCSC Ensembl
Innerchr8:6536153..6536589hg19UCSC Ensembl
Outerchr8:6535454..6536826hg19UCSC Ensembl
chr8:6523561..6523997hg18UCSC Ensembl
Innerchr8:6523561..6523997hg18UCSC Ensembl
Outerchr8:6522862..6524234hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38437
hg19437
hg18437
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4042e59
Supporting Variantsessv8652410
SamplesNA19240
Known Genes
MethodSequencing
Analysis
PlatformSOLiD
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3451275
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