A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18099135



Internal ID20666175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:4034776..4178868hg38UCSC Ensembl
chr3:4076460..4220552hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38144093
hg19144093
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6359156
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18099135
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