A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521600



Internal ID15448893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:99289771..99313871hg38UCSC Ensembl
Innerchr11:99160502..99184602hg19UCSC Ensembl
Innerchr11:98665712..98689812hg18UCSC Ensembl
Innerchr11:98665712..98689812hg17UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg3824101
hg1924101
hg1824101
hg1724101
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698217
Samples
Known GenesCNTN5
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521600
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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