A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16890049



Internal ID167501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:145414587..145421593hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg387007
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5424650
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16890049
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.002895


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