A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627694



Internal ID7014522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:109177288..109190924hg38UCSC Ensembl
chr11:109048015..109061651hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3813637
hg1913637
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv232e214
Supporting Variantsessv14278492, essv14278493
SamplesHG02682, HG02681
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627694
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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