A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4014247



Internal ID22075878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:43615147..43736980hg38UCSC Ensembl
Outerchr4:43611584..43737755hg38UCSC Ensembl
Innerchr4:43617164..43738997hg19UCSC Ensembl
Outerchr4:43613601..43739772hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg38126172
hg19126172
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156155
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4014247
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