A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519326



Internal ID15099933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:12518212..12521335hg38UCSC Ensembl
Innerchr11:12539759..12542882hg19UCSC Ensembl
Innerchr11:12496335..12499458hg18UCSC Ensembl
Innerchr11:12496335..12499458hg17UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg383124
hg193124
hg183124
hg173124
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696793
Samples
Known GenesPARVA
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519326
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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