A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3504875



Internal ID18456470
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 StatusS
Merged Variantsnsv1037294
Supporting Variants
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)nssv3504875
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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