A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154756



Internal ID22085261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:89754781..89926400hg38UCSC Ensembl
Outerchr11:89741663..89962925hg38UCSC Ensembl
Innerchr11:89487949..89659568hg19UCSC Ensembl
Outerchr11:89474831..89696093hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg38221263
hg19221263
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4007235
Samples
Known GenesMIR5692A1, TRIM49, TRIM49D1, TRIM49D2P, TRIM53AP, TRIM64B
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154756
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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