A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16295016



Internal ID20504234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:93818373..93818373hg38UCSC Ensembl
chr9:96580655..96580655hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4759306
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16295016
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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