A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528299



Internal ID15455592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:130561587..130570428hg38UCSC Ensembl
Innerchr11:130431482..130440323hg19UCSC Ensembl
Innerchr11:129936692..129945533hg18UCSC Ensembl
Innerchr11:129936692..129945533hg17UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg388842
hg198842
hg188842
hg178842
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704875
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528299
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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