A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18237098



Internal ID20804138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:125135382..125162808hg38UCSC Ensembl
chr9:127897661..127925087hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3827427
hg1927427
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6439938
Supporting Variants
Samples
Known GenesPPP6C, SCAI
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18237098
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