A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv784887



Internal ID16078843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:128805506..128813428hg38UCSC Ensembl
Innerchr11:128675401..128683323hg19UCSC Ensembl
Innerchr11:128180611..128188533hg18UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg387923
hg197923
hg187923
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv556560
Supporting Variants
Samples
Known GenesFLI1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv784887
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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