A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521880



Internal ID15449173
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:43088504..43093632hg38UCSC Ensembl
Innerchr11:43110054..43115182hg19UCSC Ensembl
Innerchr11:43066630..43071758hg18UCSC Ensembl
Innerchr11:43066630..43071758hg17UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg385129
hg195129
hg185129
hg175129
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694651
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521880
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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