A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16296708



Internal ID20505926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:78314444..78314444hg38UCSC Ensembl
chr9:80929360..80929360hg19UCSC Ensembl
Cytoband9q21.2
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4764898
Supporting Variants
Samples
Known GenesPSAT1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16296708
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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