A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521561



Internal ID15448854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:4455469..4515000hg38UCSC Ensembl
Innerchr11:4476699..4536230hg19UCSC Ensembl
Innerchr11:4433275..4492806hg18UCSC Ensembl
Innerchr11:4433275..4492806hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3859532
hg1959532
hg1859532
hg1759532
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv55n21
Supporting Variantsnssv698176
Samples
Known GenesOR52K1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521561
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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