A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6356383



Internal ID21013936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:3901324..4174086hg38UCSC Ensembl
chr4:3903051..4175813hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38272763
hg19272763
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5136n223
Supporting Variantsnssv18213571
Samples
Known GenesFAM86EP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6356383
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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