A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17525698



Internal ID21850056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:160691755..160699047hg38UCSC Ensembl
chr1:160661545..160668837hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg387293
hg197293
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5981557
Supporting Variants
Samples
Known GenesCD48
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17525698
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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