A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17590435



Internal ID21782478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:93695373..93695373hg38UCSC Ensembl
chr9:96457655..96457655hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg38144
hg19144
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6084798
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17590435
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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