A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154754



Internal ID22085259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:86178616..86187779hg38UCSC Ensembl
Outerchr11:86176915..86188770hg38UCSC Ensembl
Innerchr11:85889658..85898821hg19UCSC Ensembl
Outerchr11:85887957..85899812hg19UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg3811856
hg1911856
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv51n97
Supporting Variantsnssv4007233, nssv4007232, nssv4007231
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154754
Frequency
Sample Size131
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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