A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18171974



Internal ID20739014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:84633736..84634327hg38UCSC Ensembl
chr8:85545971..85546562hg19UCSC Ensembl
Cytoband8q21.2
Allele length
AssemblyAllele length
hg38592
hg19592
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6419320
Supporting Variants
Samples
Known GenesRALYL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18171974
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00013


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