A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18177569



Internal ID20744609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:99694701..99696000hg38UCSC Ensembl
chr9:102456983..102458282hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg381300
hg191300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6452556
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18177569
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00109


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