A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18228832



Internal ID20795872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:117413601..117415900hg38UCSC Ensembl
chr9:120175879..120178178hg19UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg382300
hg192300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6437816
Supporting Variants
Samples
Known GenesASTN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18228832
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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