A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523357



Internal ID15450650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:63033676..63071039hg38UCSC Ensembl
Innerchr11:62801148..62838511hg19UCSC Ensembl
Innerchr11:62557724..62595087hg18UCSC Ensembl
Innerchr11:62557724..62595087hg17UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg3837364
hg1937364
hg1837364
hg1737364
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699106
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523357
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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