A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18220951



Internal ID20787991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:21941401..21947300hg38UCSC Ensembl
chr8:21798912..21804811hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg385900
hg195900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6425201
Supporting Variants
Samples
Known GenesXPO7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18220951
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00031


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