A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17596547



Internal ID21788590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:128825876..128825876hg38UCSC Ensembl
chr8:129838122..129838122hg19UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg38107
hg19107
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6062899
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17596547
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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