A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155558



Internal ID22086063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:15879621..15893672hg38UCSC Ensembl
Outerchr19:15873932..15901947hg38UCSC Ensembl
Innerchr19:15990431..16004482hg19UCSC Ensembl
Outerchr19:15984742..16012757hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3828016
hg1928016
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4013459
Samples
Known GenesCYP4F2
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155558
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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