A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17015173



Internal ID77769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:109059409..109059436hg38UCSC Ensembl
chr8:110071638..110071665hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg38314
hg19314
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5537364
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17015173
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.007181


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