A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1153240



Internal ID19195945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:17053052..17058753hg38UCSC Ensembl
Outerchr11:17074599..17080300hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg385702
hg195702
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4001157
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1153240
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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