A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18230554



Internal ID20797594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:93451101..93453900hg38UCSC Ensembl
chr9:96213383..96216182hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg382800
hg192800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6452658
Supporting Variants
Samples
Known GenesFAM120A, FAM120AOS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18230554
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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