A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17593994



Internal ID21786037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:97619096..97619096hg38UCSC Ensembl
chr8:98631324..98631324hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg383709
hg193709
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6064162
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17593994
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