A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523584



Internal ID15450877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:110046434..110055714hg38UCSC Ensembl
Innerchr11:109917159..109926440hg19UCSC Ensembl
Innerchr11:109422369..109431650hg18UCSC Ensembl
Innerchr11:109422369..109431650hg17UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg389281
hg199282
hg189282
hg179282
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699373
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523584
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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