A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17520179



Internal ID21844538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:59025191..59027586hg38UCSC Ensembl
chr1:59490863..59493258hg19UCSC Ensembl
Cytoband1p32.1
Allele length
AssemblyAllele length
hg382396
hg192396
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5984536
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17520179
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