A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18092899



Internal ID20659939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:115812801..115814100hg38UCSC Ensembl
chr3:115531648..115532947hg19UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg381300
hg191300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6363801
Supporting Variants
Samples
Known GenesLSAMP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18092899
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00013


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