A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18172010



Internal ID20739050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:84884499..85034361hg38UCSC Ensembl
chr8:85796734..85946596hg19UCSC Ensembl
Cytoband8q21.2
Allele length
AssemblyAllele length
hg38149863
hg19149863
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6419109
Supporting Variants
Samples
Known GenesRALYL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18172010
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