A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154712



Internal ID22085217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:34198957..34201831hg38UCSC Ensembl
Outerchr11:34197311..34205780hg38UCSC Ensembl
Innerchr11:34220504..34223378hg19UCSC Ensembl
Outerchr11:34218858..34227327hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg388470
hg198470
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4006742, nssv4006743, nssv4006741, nssv4006744, nssv4006745
Samples
Known GenesABTB2
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154712
Frequency
Sample Size131
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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