A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6452658



Internal ID21110211
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 StatusM
Merged Variants
Supporting Variantsnssv18230554
Samples
Known GenesFAM120A, FAM120AOS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6452658
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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