A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17543095



Internal ID21867450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:150160276..150160588hg38UCSC Ensembl
chr3:149878063..149878375hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5992079
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17543095
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