A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17549986



Internal ID21874341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:65265220..65265287hg38UCSC Ensembl
chr3:65250895..65250962hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5994421
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17549986
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