A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18227059



Internal ID20794099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:41480401..41487800hg38UCSC Ensembl
chr9:68169717..68177000hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg387400
hg197284
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6448370
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18227059
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.07556


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