A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552996



Internal ID16340405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:1559798..1563495hg38UCSC Ensembl
Innerchr11:1581028..1584725hg19UCSC Ensembl
Innerchr11:1537604..1541301hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg383698
hg193698
hg183698
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv764301
Samples
Known GenesDUSP8, MOB2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552996
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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