A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3445885



Internal ID15292835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:24920317..24920330hg38UCSC Ensembl
Innerchr8:24920293..24920354hg38UCSC Ensembl
Outerchr8:24920280..24920367hg38UCSC Ensembl
chr8:24777830..24777843hg19UCSC Ensembl
Innerchr8:24777806..24777867hg19UCSC Ensembl
Outerchr8:24777793..24777880hg19UCSC Ensembl
chr8:24833735..24833748hg18UCSC Ensembl
Innerchr8:24833772..24833711hg18UCSC Ensembl
Outerchr8:24833698..24833785hg18UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg3857
hg1957
hg1857
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7864824
SamplesNA12005
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3445885
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