A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553447



Internal ID16340856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:8771075..8804419hg38UCSC Ensembl
Innerchr11:8792622..8825966hg19UCSC Ensembl
Innerchr11:8749198..8782542hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3833345
hg1933345
hg1833345
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv767050
Samples
Known GenesST5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553447
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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