A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3244241



Internal ID22375806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:123976373..123993780hg38UCSC Ensembl
chr9:126738652..126756059hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3817408
hg1917408
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9742n152
Supporting Variantsnssv14465586, nssv14466336, nssv14466190, nssv14460048, nssv14462799, nssv14460819, nssv14453612
SamplesNA19239, 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)nsv3244241
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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