A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046353



Internal ID18788884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:90255990..90332362hg38UCSC Ensembl
Innerchr11:89989158..90065530hg19UCSC Ensembl
Innerchr11:89628806..89705178hg18UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3876373
hg1976373
hg1876373
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3512867
Samples
Known GenesDISC1FP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1046353
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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