A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3302699



Internal ID15149647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:88132318..88132410hg38UCSC Ensembl
Innerchr10:88132364..88132364hg38UCSC Ensembl
Outerchr10:88132218..88132510hg38UCSC Ensembl
chr10:89892075..89892167hg19UCSC Ensembl
Innerchr10:89892121..89892121hg19UCSC Ensembl
Outerchr10:89891975..89892267hg19UCSC Ensembl
chr10:89882055..89882147hg18UCSC Ensembl
Innerchr10:89882101..89882101hg18UCSC Ensembl
Outerchr10:89881955..89882247hg18UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg3893
hg1993
hg1893
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7737403, essv7732702, essv7737678, essv7733864, essv7738242, essv7736904, essv7734150
SamplesNA10851, NA18507, NA18916, NA19138, NA12828, NA18858, NA07037
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3302699
Frequency
Sample Size185
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer