A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517447



Internal ID15444740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:63070597..63080090hg38UCSC Ensembl
Innerchr11:62838069..62847562hg19UCSC Ensembl
Innerchr11:62594645..62604138hg18UCSC Ensembl
Innerchr11:62594645..62604138hg17UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg389494
hg199494
hg189494
hg179494
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv660323, nssv676210, nssv689935, nssv681389, nssv659707, nssv654464, nssv673778, nssv697497, nssv663235, nssv671286, nssv686098, nssv663465, nssv680502, nssv652043, nssv654312, nssv657270, nssv653207, nssv687861, nssv665796, nssv660971, nssv656387
Samples
Known GenesSLC22A24
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517447
Frequency
Sample Size2026
Observed Gain0
Observed Loss21
Observed Complex0
Frequencyn/a


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