A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155901



Internal ID22086406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:192547444..192672402hg38UCSC Ensembl
Outerchr2:192543442..192673516hg38UCSC Ensembl
Innerchr2:193412170..193537128hg19UCSC Ensembl
Outerchr2:193408168..193538242hg19UCSC Ensembl
Cytoband2q32.3
Allele length
AssemblyAllele length
hg38130075
hg19130075
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4016132
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155901
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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