A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18163825



Internal ID20730865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:12805741..12974323hg38UCSC Ensembl
chr8:12663250..12831832hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg38168583
hg19168583
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6423126
Supporting Variants
Samples
Known GenesKIAA1456, LINC00681, LOC340357
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18163825
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