A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4015428



Internal ID22077059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:107144594..107155376hg38UCSC Ensembl
Outerchr4:107130343..107156277hg38UCSC Ensembl
Innerchr4:108065751..108076533hg19UCSC Ensembl
Outerchr4:108051500..108077434hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg3825935
hg1925935
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156211
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4015428
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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