A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv897188



Internal ID6304199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:31830133..31851040hg19UCSC Ensembl
Outerchr11:31826132..31856488hg19UCSC Ensembl
Innerchr11:31786709..31807616hg18UCSC Ensembl
Outerchr11:31782708..31813064hg18UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1510003
SamplesSP54956
Known GenesDKFZp686K1684, PAX6
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv897188
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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