A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17584447



Internal ID21776490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:128726819..128726819hg38UCSC Ensembl
chr8:129739065..129739065hg19UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg383344
hg193344
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6064937
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17584447
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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