A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17534231



Internal ID21858587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:108384122..108603147hg38UCSC Ensembl
chr1:108926744..109145769hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg38219026
hg19219026
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6104826
Supporting Variants
Samples
Known GenesFAM102B, NBPF6
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17534231
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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