A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6397942



Internal ID21055495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:107484040..107502595hg38UCSC Ensembl
chr5:106819741..106838296hg19UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg3818556
hg1918556
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212720
Samples
Known GenesEFNA5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6397942
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