A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18121358



Internal ID20688398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:99894201..99894800hg38UCSC Ensembl
chr4:100815358..100815957hg19UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg38600
hg19600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6381959
Supporting Variants
Samples
Known GenesLAMTOR3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18121358
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.06967


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