A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17583982



Internal ID21776025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:90476333..90476333hg38UCSC Ensembl
chr8:91488561..91488561hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg38462
hg19462
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6080042
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17583982
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