A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4017374



Internal ID22079005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:3461725..3485595hg38UCSC Ensembl
Outerchr4:3453009..3502209hg38UCSC Ensembl
Innerchr4:3463452..3487322hg19UCSC Ensembl
Outerchr4:3454736..3503936hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3849201
hg1949201
Variant TypeCNV duplication
Copy Number4
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156081
Supporting Variants
Samples
Known GenesDOK7
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4017374
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