A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5981458



Internal ID21890801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:153668698..153668755hg38UCSC Ensembl
chr1:153641174..153641231hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17519114
Samples
Known GenesILF2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5981458
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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