A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7737365



Internal ID14367692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:58080546..58132753hg38UCSC Ensembl
Outerchr10:58080346..58132953hg38UCSC Ensembl
Innerchr10:59840306..59892514hg19UCSC Ensembl
Outerchr10:59840106..59892714hg19UCSC Ensembl
Innerchr10:59510312..59562520hg18UCSC Ensembl
Outerchr10:59510112..59562720hg18UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg3852608
hg1952609
hg1852609
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3302840
Supporting Variants
SamplesNA18858
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7737365
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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