A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17009772



Internal ID74159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:42226318..42268730hg38UCSC Ensembl
chr8:42083836..42126248hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg3842413
hg1942413
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5475903
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17009772
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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