A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7732702



Internal ID14445484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:88132364..88132365hg38UCSC Ensembl
Outerchr10:88132219..88132510hg38UCSC Ensembl
Innerchr10:89892121..89892122hg19UCSC Ensembl
Outerchr10:89891976..89892267hg19UCSC Ensembl
Innerchr10:89882102..89882101hg18UCSC Ensembl
Outerchr10:89881956..89882247hg18UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg38292
hg19292
hg18292
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3302699
Supporting Variants
SamplesNA18916
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7732702
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