A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5984562



Internal ID21893905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:42181812..42181866hg38UCSC Ensembl
chr1:42647483..42647537hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17526274
Samples
Known GenesFOXJ3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5984562
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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