A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16280741



Internal ID20489959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:135518657..135518657hg38UCSC Ensembl
chr9:138410503..138410503hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4766620
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16280741
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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