A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17559839



Internal ID21884194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:30362752..30363014hg38UCSC Ensembl
chr8:30220268..30220530hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38263
hg19263
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6012686
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17559839
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer