A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6355283



Internal ID21012836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:197559974..197655410hg38UCSC Ensembl
chr2:198424698..198520134hg19UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg3895437
hg1995437
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18208254
Samples
Known GenesRFTN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6355283
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