A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17541129



Internal ID21865484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:188203404..188203540hg38UCSC Ensembl
chr3:187921192..187921328hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg38137
hg19137
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5992223
Supporting Variants
Samples
Known GenesLPP
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17541129
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