A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17520555



Internal ID21844914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:216804406..216804406hg38UCSC Ensembl
chr2:217669129..217669129hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg38142
hg19142
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6040852
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17520555
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