A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156408



Internal ID22086809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:168866887..168872192hg38UCSC Ensembl
Outerchr5:168863624..168878099hg38UCSC Ensembl
Innerchr5:168293892..168299197hg19UCSC Ensembl
Outerchr5:168290629..168305104hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg3814476
hg1914476
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4016721
Samples
Known GenesSLIT3
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156408
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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