A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18166081



Internal ID20733121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:21571556..21572029hg38UCSC Ensembl
chr8:21429067..21429540hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg38474
hg19474
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6418032
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18166081
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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