A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5981084



Internal ID21890427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:143327460..143327618hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38159
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17524568
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5981084
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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