A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8688150



Internal ID13633354
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:89038215..89042613hg38UCSC Ensembl
Innerchr10:89039215..89041613hg38UCSC Ensembl
Outerchr10:89037215..89043613hg38UCSC Ensembl
chr10:90797972..90802370hg19UCSC Ensembl
Innerchr10:90798972..90801370hg19UCSC Ensembl
Outerchr10:90796972..90803370hg19UCSC Ensembl
chr10:90787952..90792350hg18UCSC Ensembl
Innerchr10:90788952..90791350hg18UCSC Ensembl
Outerchr10:90786952..90793350hg18UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg384399
hg194399
hg184399
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv3368471
Supporting Variants
SamplesNA12878
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8688150
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