A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5981300



Internal ID21890643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:143257483..143257534hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3852
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17521588
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5981300
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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