A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18229790



Internal ID20796831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:86945801..86949100hg38UCSC Ensembl
chr9:89560716..89564015hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg383300
hg193300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6439259
Supporting Variants
Samples
Known GenesGAS1, LOC100506834
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18229790
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00015


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