A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17035775



Internal ID91596
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:53216961..53445959hg38UCSC Ensembl
chr10:54976721..55205719hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38228999
hg19228999
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5480532
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17035775
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