A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1153289



Internal ID19197492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:57807220..57809220hg38UCSC Ensembl
Outerchr11:57574692..57576692hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg382001
hg192001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4001208
SamplesKWB1
Known GenesCTNND1, TMX2-CTNND1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1153289
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