A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18094114



Internal ID20661154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:127773519..127775848hg38UCSC Ensembl
chr3:127492362..127494691hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg382330
hg192330
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6374692
Supporting Variants
Samples
Known GenesMGLL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18094114
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