A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154783



Internal ID22085288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:128310915..128312747hg38UCSC Ensembl
Outerchr11:128309181..128319206hg38UCSC Ensembl
Innerchr11:128180810..128182642hg19UCSC Ensembl
Outerchr11:128179076..128189101hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg3810026
hg1910026
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4007325
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154783
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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