A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17584026



Internal ID21776069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:60778952..60779011hg38UCSC Ensembl
chr10:62538710..62538769hg19UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6002248
Supporting Variants
Samples
Known GenesCDK1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17584026
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