A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7731108



Internal ID13700573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:73999068..73999146hg38UCSC Ensembl
Innerchr11:73999106..73999107hg38UCSC Ensembl
Outerchr11:73998968..73999246hg38UCSC Ensembl
chr11:73710113..73710191hg19UCSC Ensembl
Innerchr11:73710151..73710152hg19UCSC Ensembl
Outerchr11:73710013..73710291hg19UCSC Ensembl
chr11:73387761..73387839hg18UCSC Ensembl
Innerchr11:73387800..73387799hg18UCSC Ensembl
Outerchr11:73387661..73387939hg18UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg3879
hg1979
hg1879
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3302642
Supporting Variants
SamplesNA12891
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7731108
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