A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18216721



Internal ID20783761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:159677163..159681342hg38UCSC Ensembl
chr6:160098195..160102374hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg384180
hg194180
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6615447
Supporting Variants
Samples
Known GenesSOD2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18216721
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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