A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521169



Internal ID15448462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:9908687..9909346hg38UCSC Ensembl
Innerchr11:9930234..9930893hg19UCSC Ensembl
Innerchr11:9886810..9887469hg18UCSC Ensembl
Innerchr11:9886810..9887469hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38660
hg19660
hg18660
hg17660
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv686483, nssv683800
Samples
Known GenesSBF2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521169
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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