A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18168403



Internal ID20735443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:53905580..53910323hg38UCSC Ensembl
chr8:54818140..54822883hg19UCSC Ensembl
Cytoband8q11.23
Allele length
AssemblyAllele length
hg384744
hg194744
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6419905
Supporting Variants
Samples
Known GenesRGS20
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18168403
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