A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520324



Internal ID15447617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:12574460..12584561hg38UCSC Ensembl
Innerchr11:12596007..12606108hg19UCSC Ensembl
Innerchr11:12552583..12562684hg18UCSC Ensembl
Innerchr11:12552583..12562684hg17UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg3810102
hg1910102
hg1810102
hg1710102
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv662922, nssv690094
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520324
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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