A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552989



Internal ID15993712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:1494864..1554849hg38UCSC Ensembl
Innerchr11:1516094..1576079hg19UCSC Ensembl
Innerchr11:1472670..1532655hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3859986
hg1959986
hg1859986
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv764285
Samples
Known GenesDUSP8, MOB2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552989
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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