A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18098281



Internal ID20665321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:21932401..21945200hg38UCSC Ensembl
chr3:21973893..21986692hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3812800
hg1912800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6361645
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18098281
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