A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521616



Internal ID15448909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:11102109..11145046hg38UCSC Ensembl
Innerchr11:11123656..11166593hg19UCSC Ensembl
Innerchr11:11080232..11123169hg18UCSC Ensembl
Innerchr11:11080232..11123169hg17UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg3842938
hg1942938
hg1842938
hg1742938
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698234
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521616
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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