A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17538329



Internal ID21862684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:45101727..45101835hg38UCSC Ensembl
chr3:45143219..45143327hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg38109
hg19109
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5993468
Supporting Variants
Samples
Known GenesCDCP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17538329
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