A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16281843



Internal ID20491061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:112138235..112138235hg38UCSC Ensembl
chr9:114900515..114900515hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg38115
hg19115
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4764197
Supporting Variants
Samples
Known GenesMIR3134, SUSD1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16281843
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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