A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17544933



Internal ID21869288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:129971760..129971760hg38UCSC Ensembl
chr3:129690603..129690603hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6067212
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17544933
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer