A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18226881



Internal ID20793921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:89409625..89410551hg38UCSC Ensembl
chr9:92024540..92025466hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg38927
hg19927
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6453314
Supporting Variants
Samples
Known GenesSEMA4D
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18226881
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