A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18172573



Internal ID20739613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:103718832..103720378hg38UCSC Ensembl
chr9:106481114..106482660hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg381547
hg191547
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6437035
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18172573
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