A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18095215



Internal ID20662255
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:122831965..122832636hg38UCSC Ensembl
chr3:122550812..122551483hg19UCSC Ensembl
Cytoband3q21.1
Allele length
AssemblyAllele length
hg38672
hg19672
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6367551
Supporting Variants
Samples
Known GenesDIRC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18095215
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00016


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