A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3302840



Internal ID15149788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:58080445..58132853hg38UCSC Ensembl
Innerchr10:58080545..58132753hg38UCSC Ensembl
Outerchr10:58080345..58132953hg38UCSC Ensembl
chr10:59840205..59892614hg19UCSC Ensembl
Innerchr10:59840305..59892514hg19UCSC Ensembl
Outerchr10:59840105..59892714hg19UCSC Ensembl
chr10:59510211..59562620hg18UCSC Ensembl
Innerchr10:59510311..59562520hg18UCSC Ensembl
Outerchr10:59510111..59562720hg18UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg3852409
hg1952410
hg1852410
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7737365
SamplesNA18858
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3302840
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