A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6407254



Internal ID21064807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:99497401..99539400hg38UCSC Ensembl
chr5:98833105..98875104hg19UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg3842000
hg1942000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5836n223
Supporting Variantsnssv18215479
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6407254
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