A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14091004



Internal ID21268314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:129667265..129758857hg38UCSC Ensembl
Innerchr11:129537160..129628752hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg3891593
hg1991593
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3112330
Supporting Variants
Samplessample123
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14091004
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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