A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8688490



Internal ID14665657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65834005..65835203hg38UCSC Ensembl
Innerchr11:65834203..65835005hg38UCSC Ensembl
Outerchr11:65833005..65836203hg38UCSC Ensembl
chr11:65601476..65602674hg19UCSC Ensembl
Innerchr11:65601674..65602476hg19UCSC Ensembl
Outerchr11:65600476..65603674hg19UCSC Ensembl
chr11:65358052..65359250hg18UCSC Ensembl
Innerchr11:65359052..65358250hg18UCSC Ensembl
Outerchr11:65357052..65360250hg18UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg381199
hg191199
hg181199
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3364341
Supporting Variants
SamplesNA19238
Known GenesSNX32
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8688490
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