A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3548540



Internal ID18402930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:132213736..132214025hg38UCSC Ensembl
Outerchr11:132213677..132214080hg38UCSC Ensembl
Innerchr11:132083630..132083919hg19UCSC Ensembl
Outerchr11:132083571..132083974hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38404
hg19404
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9747287
Samples
Known GenesNTM
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3548540
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