A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17580680



Internal ID21772723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:109337068..109337068hg38UCSC Ensembl
chr8:110349297..110349297hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6064183
Supporting Variants
Samples
Known GenesENY2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17580680
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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