A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18169061



Internal ID20736101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:54490663..54499061hg38UCSC Ensembl
chr8:55403223..55411621hg19UCSC Ensembl
Cytoband8q11.23
Allele length
AssemblyAllele length
hg388399
hg198399
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6424679
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18169061
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