A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4014727



Internal ID22076358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:96399079..96401252hg38UCSC Ensembl
Outerchr4:96395896..96405817hg38UCSC Ensembl
Innerchr4:97320230..97322403hg19UCSC Ensembl
Outerchr4:97317047..97326968hg19UCSC Ensembl
Cytoband4q22.3
Allele length
AssemblyAllele length
hg389922
hg199922
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156202
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4014727
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer