A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18099983



Internal ID20667023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:43916114..43973519hg38UCSC Ensembl
chr3:43957606..44015011hg19UCSC Ensembl
Cytoband3p21.33
Allele length
AssemblyAllele length
hg3857406
hg1957406
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6373068
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18099983
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