A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516406



Internal ID15443699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:28705017..28761637hg38UCSC Ensembl
Innerchr11:28726564..28783184hg19UCSC Ensembl
Innerchr11:28683140..28739760hg18UCSC Ensembl
Innerchr11:28683140..28739760hg17UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg3856621
hg1956621
hg1856621
hg1756621
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv674583, nssv668124
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516406
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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