A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17531956



Internal ID21856312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:162042488..162052885hg38UCSC Ensembl
chr1:162012278..162022675hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg3810398
hg1910398
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6102345
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17531956
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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