A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18190974



Internal ID20758014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:99269861..99270578hg38UCSC Ensembl
chr9:102032143..102032860hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg38718
hg19718
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6440722
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18190974
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00036


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