A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515891



Internal ID15442948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:9254351..9313414hg38UCSC Ensembl
Innerchr11:9275898..9334961hg19UCSC Ensembl
Innerchr11:9232474..9291537hg18UCSC Ensembl
Innerchr11:9232474..9291537hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3859064
hg1959064
hg1859064
hg1759064
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv666294, nssv665166
Samples
Known GenesDENND5A, TMEM41B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515891
Frequency
Sample Size2026
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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