A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3545212



Internal ID22414229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:41768334..42093866hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38325533
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14464263, nssv14453412, nssv14455700, nssv14465096, nssv14458167, nssv14463712, nssv14464854, nssv14456123, nssv14463941
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisSingle strand sequencing, and assortment analysis
PlatformStrand-seq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3545212
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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