A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17033459



Internal ID89994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:28993666..28994797hg38UCSC Ensembl
chr10:29282595..29283726hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg381132
hg191132
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5490643
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17033459
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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