A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4005538



Internal ID22067169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:4228783..4315299hg38UCSC Ensembl
Outerchr11:4217824..4325579hg38UCSC Ensembl
Innerchr11:4250013..4336529hg19UCSC Ensembl
Outerchr11:4239054..4346809hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38107756
hg19107756
Variant TypeCNV duplication
Copy Number4
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1154671
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4005538
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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