A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526546



Internal ID15453839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:93009020..93118012hg38UCSC Ensembl
Innerchr11:92742186..92851178hg19UCSC Ensembl
Innerchr11:92381834..92490826hg18UCSC Ensembl
Innerchr11:92381834..92490826hg17UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg38108993
hg19108993
hg18108993
hg17108993
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702860
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526546
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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