A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16890051



Internal ID167503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:145443293..145473587hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3830295
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6138491
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16890051
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.002414


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