A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516461



Internal ID15097068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:93498310..93507681hg38UCSC Ensembl
Innerchr11:93231476..93240847hg19UCSC Ensembl
Innerchr11:92871124..92880495hg18UCSC Ensembl
Innerchr11:92871124..92880495hg17UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg389372
hg199372
hg189372
hg179372
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv79n21
Supporting Variantsnssv692144, nssv668537, nssv674405, nssv680533, nssv676924
Samples
Known GenesSMCO4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516461
Frequency
Sample Size2026
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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