A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625763



Internal ID6665911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:27084023..27085631hg38UCSC Ensembl
Innerchr11:27084041..27085614hg38UCSC Ensembl
Outerchr11:27084006..27085649hg38UCSC Ensembl
chr11:27105570..27107178hg19UCSC Ensembl
Innerchr11:27105588..27107161hg19UCSC Ensembl
Outerchr11:27105553..27107196hg19UCSC Ensembl
Cytoband11p14.2
Allele length
AssemblyAllele length
hg381609
hg191609
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14071730
SamplesHG00445
Known GenesBBOX1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625763
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer