A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154747



Internal ID22085252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:71479586..71481754hg38UCSC Ensembl
Outerchr11:71471313..71484605hg38UCSC Ensembl
Innerchr11:71190632..71192800hg19UCSC Ensembl
Outerchr11:71182359..71195651hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg3813293
hg1913293
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4007201
Samples
Known GenesMIR6754, NADSYN1
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154747
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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