A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522057



Internal ID15449350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:98285990..98471737hg38UCSC Ensembl
Innerchr11:98156718..98342466hg19UCSC Ensembl
Innerchr11:97661928..97847676hg18UCSC Ensembl
Innerchr11:97661928..97847676hg17UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg38185748
hg19185749
hg18185749
hg17185749
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694828
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522057
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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