A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3545336



Internal ID18399726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:113105328..113106806hg38UCSC Ensembl
chr9:115867608..115869086hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg381479
hg191479
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9744083
Samples
Known GenesFAM225B
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3545336
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