A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037294



Internal ID18779825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:134260280..134340956hg38UCSC Ensembl
Innerchr11:134130174..134210850hg19UCSC Ensembl
Innerchr11:133635384..133716060hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3880677
hg1980677
hg1880677
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3504875
Samples
Known GenesACAD8, GLB1L2, GLB1L3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1037294
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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