A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18140255



Internal ID20707295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:14379765..14380910hg38UCSC Ensembl
chr6:14379996..14381141hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg381146
hg191146
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6413705
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18140255
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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