A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525366



Internal ID15452659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:99619715..99634939hg38UCSC Ensembl
Innerchr11:99490446..99505670hg19UCSC Ensembl
Innerchr11:98995656..99010880hg18UCSC Ensembl
Innerchr11:98995656..99010880hg17UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg3815225
hg1915225
hg1815225
hg1715225
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701486
Samples
Known GenesCNTN5
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525366
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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