A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156171



Internal ID22086676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:65707409..65764267hg38UCSC Ensembl
Outerchr4:65706722..65767139hg38UCSC Ensembl
Innerchr4:66573127..66629985hg19UCSC Ensembl
Outerchr4:66572440..66632857hg19UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg3860418
hg1960418
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4016509
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156171
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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