A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1152940



Internal ID18850471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:117320447..117320615hg38UCSC Ensembl
Outerchr11:117191163..117191331hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38169
hg19169
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3997975
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1152940
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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