A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516460



Internal ID15097067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:62337465..62386689hg38UCSC Ensembl
Innerchr11:62104937..62154161hg19UCSC Ensembl
Innerchr11:61861513..61910737hg18UCSC Ensembl
Innerchr11:61861513..61910737hg17UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg3849225
hg1949225
hg1849225
hg1749225
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv672300, nssv668534
Samples
Known GenesASRGL1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516460
Frequency
Sample Size2026
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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