A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521581



Internal ID15102188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:134126584..134772738hg38UCSC Ensembl
Innerchr11:133996479..134642632hg19UCSC Ensembl
Innerchr11:133501689..134147842hg18UCSC Ensembl
Innerchr11:133501689..134147842hg17UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38646155
hg19646154
hg18646154
hg17646154
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698196
Samples
Known GenesACAD8, B3GAT1, GLB1L2, GLB1L3, JAM3, LOC283177, NCAPD3, THYN1, VPS26B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521581
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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