A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9746026



Internal ID18720272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:7407386..7407633hg38UCSC Ensembl
Outerchr11:7407311..7407735hg38UCSC Ensembl
Innerchr11:7428617..7428864hg19UCSC Ensembl
Outerchr11:7428542..7428966hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38425
hg19425
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3547279
Supporting Variants
Samples
Known GenesSYT9
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9746026
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