A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17517721



Internal ID21842080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:45710769..45711045hg38UCSC Ensembl
chr1:46176441..46176717hg19UCSC Ensembl
Cytoband1p34.1
Allele length
AssemblyAllele length
hg38277
hg19277
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5984255
Supporting Variants
Samples
Known GenesIPP
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17517721
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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