A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553476



Internal ID16340885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:10002764..10095888hg38UCSC Ensembl
Innerchr11:10024311..10117435hg19UCSC Ensembl
Innerchr11:9980887..10074011hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3893125
hg1993125
hg1893125
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv767790
Samples
Known GenesSBF2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553476
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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