A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528911



Internal ID15456204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55315958..55388958hg38UCSC Ensembl
Innerchr11:55083434..55156434hg19UCSC Ensembl
Innerchr11:54840010..54913010hg18UCSC Ensembl
Innerchr11:54840010..54913010hg17UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3873001
hg1973001
hg1873001
hg1773001
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv68n21
Supporting Variantsnssv705596
Samples
Known GenesOR4A15, OR4A16
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528911
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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