A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18145820



Internal ID20712860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:5566294..5584175hg38UCSC Ensembl
chr6:5566527..5584408hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg3817882
hg1917882
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6397888
Supporting Variants
Samples
Known GenesFARS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18145820
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00033


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