A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17519509



Internal ID21843868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:42222034..42222034hg38UCSC Ensembl
chr1:42687705..42687705hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg38223
hg19223
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6051832
Supporting Variants
Samples
Known GenesFOXJ3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17519509
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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