A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18236987



Internal ID20804028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:128408486..128409502hg38UCSC Ensembl
chr9:131170765..131171781hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg381017
hg191017
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6441113
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18236987
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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