A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154693



Internal ID22085198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:10489595..10515370hg38UCSC Ensembl
Outerchr11:10485237..10518796hg38UCSC Ensembl
Innerchr11:10511142..10536917hg19UCSC Ensembl
Outerchr11:10506784..10540343hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3833560
hg1933560
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4005751
Samples
Known GenesAMPD3, MIR4485, MTRNR2L8, RNF141
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154693
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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