A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3559683



Internal ID18414073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:18268816..18268870hg38UCSC Ensembl
chr11:18290363..18290417hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv54e215
Supporting Variantsessv9758430
Samples
Known GenesSAA1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3559683
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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