A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18094804



Internal ID20661844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:133708735..133711304hg38UCSC Ensembl
chr3:133427579..133430148hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg382570
hg192570
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6359277
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18094804
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