A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17850628



Internal ID22034271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:53613709..53613709hg38UCSC Ensembl
chr20:52230248..52230248hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6251525
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17850628
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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